Burger Reviews BTK Inhibitors and Beyond in Frontline CLL – Targeted Oncology

During a virtual Case Based Peer Perspectives event, Jan A. Burger, MD, PhD, professor, Department of Leukemia, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center in Houston, TX, discussed testing and the treatment options for chronic lymphocytic leukemia (CLL), based on the a case of 71-year-old female patient.

Targeted OncologyTM: What testing would you order to confirm diagnosis if you saw this patient in the clinic?

BURGER: We need to establish the diagnosis by flow cytometry and then we would do, at a minimum, FISH cytogenetics and, ideally, the mutational status. Cytogenetics can change, but mutational status usually doesnt change. If thats been established somewhere outside [of your clinic], then you dont have to repeat that test.

Its important to repeat cytogenetics if you talk about the relapse setting. But here, were treating in the frontline setting, and she was tested. She was found to be IGHV unmutated and [positive for] del(11q). That, traditionally, has been regarded as a higher-risk disease status because these patients respond OK to standard chemotherapy, but they have short remissions and survival times with FCR [fludarabine, cyclophosphamide, and rituximab (Rituxan)], BR [bendamustine plus rituximab], and those kinds of regimens compared with low-risk patients, such as those [who are positive for] deletion 13q and have IGHV mutated disease.

In terms of these sequences, when you see a patient with lymphocytosis, you send for flow cytometry, and part of the flow cytometry panel can test for additional markers, CD38 and ZAP-70. We have it [at MD Anderson], but Im not sure if there are any outside routine flow cytometry labs reporting CD38 positivity or negativity or ZAP-70. These markers used to be very popular 10 years or so ago when IGHV-mutation status was not so commonly done and was more complicated to get. Nowadays, theres a shift with sending a sample directly for IGHV-mutation testing.

If you have that and the routine CLL FISH panel, then you have a good amount of information about your patient to say this is high-, low-, or an intermediate-risk disease. I think the main purpose for doing these is, first, to identify [patients with] high-risk disease who have a deletion 17p [del(17p)] or TP53 mutations. If its a young patient, you want to know that to [be able to] avoid chemotherapy. If its a young patient, [you may want to] send those patients for evaluation for stem cell transplant. For some patients, that is still something that eventually needs to be considered for those with del(17p).

What systemic therapy would you offer?

If you have treated with ibrutinib [Imbruvica] and youre comfortable with that, I dont think at this time there is a strong reason to change. In selected patients, it might be reasonable to try switching them from one [agent] to the other. But right now, for this patient, consensus says a BTK [Bruton tyrosine kinase] inhibitor is a good treatment.

Both ibrutinib and acalabrutinib [Calquence] can be used as single agents or in combination with CD20 antibodies. Weve done a clinical study with ibrutinib where patients were randomized to receive monotherapy versus a combination with rituximab, and the outcome was virtually identicalwhere patients had the exact same progression-free survival [PFS] with a single agent versus the combination with a CD20 antibody.1

CD20 antibodies with BTK inhibitors dont seem to add benefit in terms of survival if you go with the long-term BTK inhibitor treatment and if youre not planning to stop your treatment at some point. What they do is they get patients into remission faster and you clear the disease faster if you add a CD20 antibody, but then you stop after 6 months. You continue your BTK inhibitor, and patients do great 2, 3, and 4 years later. Then, you dont see any effect in terms of longer-term PFS or overall survival [OS] from the addition of the CD20 antibody.

What data support the use of single-agent ibrutinib in patients with untreated CLL?

There are data from the RESONATE-2 study [NCT01722487], which randomized patients between ibrutinib and chlorambucil. This study was designed at the time when chlorambucil monotherapy was still the standard of care. Patients were randomized 1:1, and patients with del(17p) were excluded.2

What is nice about this study is that we have a long follow-up now.3 At the 5-year follow-up, you see this major difference in terms of PFS [HR, 0.146; 95% CI, 0.098-0.218]. There is also an overall survival benefit [HR, 0.450; 95% CI, 0.266-0.761].

What [we saw was] that patients with del(11q) seemed to have a better PFS than those patients who lack del(11q) when they are treated with ibrutinib. Patients with del(11q) who are treated with chemotherapy do not do as well as those who lack this cytogenetic abnormality. The same is true here for [IGHV] mutational status.

The PCYC-1102-CA study [NCT01105247] opened around 2010, and we now have 7 to 8 years of follow-up. If you use a BTK inhibitor in the frontline setting, you can expect that most patients are going to do well for an extended period of time. At 5, 6, and 7 years or longer, 70% to 80% of patients are still in remission and have not died.4

Another randomized study that created some waves [is the E1912 study (NCT02048813)]. Weve been big proponents of FCR, which was the comparator arm [of this trial] versus ibrutinib. Patients receive either 6 cycles FCR or continuous ibrutinib [with rituximab] for the first 6 cycles.5

That study showed that compared with FCR, there was a significant increase in PFS [HR, 0.39; 95% CI, 0.26-0.57; P <.0001] but also in OS benefit from the BTK inhibitorcontaining regimen [HR, 0.34; 95% CI, 0.15-0.79; P = .009].

Would you say ibrutinib is the standard of care for treatment of CLL in the frontline setting?

Ibrutinib monotherapy, I would say, is the standard of care, but ibrutinib plus rituximab can be used. Some of you use it and, based on the data we just saw, the FDA has now officially approved it.6 It doesnt mean you must use rituximab.

What other ibrutinib combinations are available?

The ALLIANCE trial [NCT01886872] had a single-agent ibrutinib arm versus ibrutinib plus rituximab versus bendamustine plus rituximab.7 When you have patients randomized to receive ibrutinib/rituximab versus ibrutinib as a single agent, the [Kaplan-Meier survival] curves are basically identical, and thats what we got as well in a slightly diff erent patient population, mostly relapsed patients. In terms of PFS, rituximab doesnt seem to add very much when you go with continuous ibrutinib treatment. You see the difference for bendamustine/rituximab, with which patients have significantly shorter PFS.

I think the theme is the same over and over again with these randomized studies. With the new targeted agents, such as the BTK inhibitors and venetoclax [Venclexta], we see the same pattern. The new agents are doing better than our traditional chemoimmunotherapy.

ILLUMINATE [NCT02264574] is the study comparing ibrutinib/obinutuzumab [Gazyva] with another chemoimmunotherapy regimen, which has been somewhat popular for older populations, more frail patients for whom you dont want to use FCR or BR. You traditionally use chlorambucil alone and then more recentlyits combined with CD20 antibodies. The patients were randomized to either [ibrutinib/obinutuzumab] versus chlorambucil/obinutuzumab treatment.8

The results show a major PFS benefits for patients on the BTK inhibitor [HR, 0.23; 95% CI, 0.15-0.37; P < .0001]. There was a big difference for genetically high-risk patients [HR, 0.15; P < .0001] or patients who had bulky disease.

What other BTK inhibitors would you consider here?

Now were going to the second-generation BTK inhibitor, acalabrutinib [Calquence], which is somewhat more selective and doesnt inhibit some other kinases that ibrutinib does. Its a new BTK inhibitor with not as much long-term follow-up data available.

[In the phase 3 ELEVATE TN trial (NCT02475681)], you have 3 arms: single-agent acalabrutinib, acalabrutinib combined with obinutuzumab, and the comparator arm of chlorambucil/obinutuzumab. 9 If you give that to treatment-nave patients, those receiving BTK inhibitor alone or with the CD20 antibody do well. Its debatable if the PFS difference is significant, but clearly, the BTK inhibitortreated patients do much better than those receiving chlorambucil plus obinutuzumab.

[If you look at the] subgroups of patients benefitting from the BTK inhibitor treatment versus obinutuzumab/chlorambucil, it basically shows that all subgroups have benefit. Some may be a little more than others...but I think particularly patients that we traditionally called high risk are the ones who benefit the most from new agents. Theres less difference if you go into the lowrisk patient populations.

Are there data supporting the use of a BCL2 inhibition?

The other frontline option involves venetoclax, and thats coming from this CLL14 trial [NCT02242942]. Patients were receiving venetoclax/obinutuzumab or chlorambucil/obinutuzumab, and this is a finite treatment for 12 months. These are patients who were older and who have some comorbidities. Deletion(17p) was not excluded.10

There is a major difference in PFS favoring the new targeted agent venetoclax. Now its approved for the frontline treatment of selected patients,11 but you can also see in comparison to the BTK inhibitors [that] the follow-up is relatively short of 3 years.

With venetoclax, you get more complete remissions and some of these remissions are MRD [minimal residual disease] negative. As long as these differences are not translating into a survival benefit, those are just numbers.

Would you recommend venetoclax after the first line?

I dont think theres a reason to make that change [from BTK inhibitors] because venetoclax has its own issues in terms of how its used and adverse effects [AEs]. For that questionmaybe [we ask [is] venetoclax better in terms of outcome than a BTK inhibitor?

Its difficult to be better than the BTK inhibitor in the frontline CLL setting, and you need a very long follow-up to show any differences if there are any.

A substantial number of patients [treated with venetoclax] receive MRD-negative remissions with this combination. MRD negativity doesnt mean patients are cured. There is drop off in PFS, so MRD negativity doesnt mean those patients will survive and never need treatment again. Most likely, those patients eventually will lose MRD and eventually have disease progression and need treatment again. I think for those studies based on frontline venetoclax for 12 months, we just have to stay tuned and wait for what the long-term outcome is going to be.

What are the AEs of venetoclax?

You see more AEs that are reminiscent of chemotherapy days, where patients get more cytopenia. Its well established that venetoclax is myelosuppressive. Certainly, neutropenia can be seen, and less frequently, thrombocytopenia and anemia. If you treat a patient with venetoclax with or without a CD20 antibody, then you have to prepare for some patients having issues with neutropenia and some who cannot be fully dose-escalated because of those cytopenias.

If the patient was younger, would you treat differently?

My answer would be no. I dont see any difference. This patient was 71 years old. We wouldnt use chemoimmunotherapy.

Somebody voted no. I think thats interesting because its something Im interested in [finding out about]. Im wondering if we have to accept treating patients with BTK inhibitorsfor very long periods or if we can maybe try it at least as an alternative treatment just for a certain period of time until we have the best response. Then, some patients maybe stop. I think thats interesting for a clinical trial.

Outside of clinical trials, Im not so sure. We have no data. But if you have a low-risk patient and you want to stop after 2 years and just see what happens, you need to tell the patient we dont know whats going to happen and you have to watch that patient more closely. If its a patient with del(17p), a high-risk patient who was very symptomatic, I wouldnt do that. But in low-risk patients, I think its an interesting question and not totally unreasonable.

Over time, we will find new solutions. Everybodys working on transitioning BTK inhibitorsto limited-duration treatments for many reasons. Its not the optimal situation to have patients on kinase inhibitors for 5, 10, or 20 years. Right now, its a long-term treatment until we have better treatments.

References:

1. Burger JA, Sivina M, Jain N, et al. Randomized trial of ibrutinib vs ibrutinib plus rituximab in patients with chronic lymphocytic leukemia. Blood. 2019;133(10):1011-1019. doi:10.1182/blood-2018-10-879429

2. Burger JA, Tedeschi A, Barr PM, et al. Ibrutinib as initial therapy for patients with chronic lymphocytic leukemia. N Engl J Med. 2015;373(25):2425-2437. doi:10.1056/NEJMoa1509388

3. Burger JA, Barr PM, Robak T, et al. Long-term effi cacy and safety of fi rst-line ibrutinib treatment for patients with CLL/SLL: 5 years of follow-up from the phase 3 RESONATE-2 study. Leukemia. 2020;34(3):787-798. doi:10.1038/s41375-019-0602-x

4. Byrd JC, Furman RR, Coutre SE, et al. Ibrutinib treatment for fi rst-line and relapsed/ refractory chronic lymphocytic leukemia: fi nal analysis of the pivotal phase Ib/II PCYC- 1102 study. Clin Cancer Res. Published online March 24, 2020. doi:10.1158/1078-0432.CCR-19-2856

5. Shanafelt TD, Wang XV, Kay NE, et al. Ibrutinib and rituximab provides superior clinical outcome compared to FCR in younger patients with chronic lymphocytic leukemia (CLL): extended follow-up from the E1912 Trial. Blood. 2019;134(suppl 1):33. doi:10.1182/blood-2019-126824

6. FDA approves ibrutinib plus rituximab for chronic lymphocytic leukemia. News release. FDA. April 21, 2020. Accessed July 27, 2020. https://bit.ly/3jV1hGW

7. Woyach JA, Ruppert AS, Heerema NA, et al. Ibrutinib regimens versus chemoimmunotherapy in older patients with untreated CLL. N Engl J Med. 2018;379(26):2517-2528. doi:10.1056/NEJMoa1812836

8. Moreno C, Greil R, Demirkan F, et al. Ibrutinib plus obinutuzumab versus chlorambucil plus obinutuzumab in fi rst-line treatment of chronic lymphocytic leukaemia (iLLUMINATE): a multicentre, randomised, open-label, phase 3 trial. Lancet Oncol. 2019;20(1):43-56. Published correction appears in Lancet Oncol. 2019;20(1):e10. doi:10.1016/S1470-2045(18)30788-5

9. Sharman JP, Egyed M, Jurczak W, et al. Acalabrutinib with or without obinutuzumab versus chlorambucil and obinutuzmab for treatment-naive chronic lymphocytic leukaemia (ELEVATE TN): a randomised, controlled, phase 3 trial. Lancet. 2020;395(10232):1278-1291. Published correction appears in Lancet. 2020;395(10238):1694. doi:10.1016/S0140-6736(20)30262-2

10. Fischer K, Al-Sawaf O, Bahlo J, et al. Venetoclax and obinutuzumab in patients with CLL and coexisting conditions. N Engl J Med. 2019;380(23):2225-2236. doi:10.1056/NEJMoa1815281

11. FDA approves venetoclax for CLL and SLL. News release. FDA. May 15, 2019.Accessed July 27, 2020. https://bit.ly/3jLnEOU

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Burger Reviews BTK Inhibitors and Beyond in Frontline CLL - Targeted Oncology

Adapting ideas from quantum physics to calculate alternative interventions for infection and cancer – Science Codex

CLEVELAND - Published in Nature Physics, findings from a new study co-led by Cleveland Clinic and Case Western Reserve University teams show for the first time how ideas from quantum physics can help develop novel drug interventions for bacterial infections and cancer.

The research team demonstrated that principles of quantum control, a field of quantum physics used in computing applications, can be translated and applied to biological problems. They constructed a mathematical algorithm that can be used to design and speed-up specific interventions to prevent or overturn drug resistance.

Typically cells in the presence of drugs evolve according to Darwinian natural selection: mutants that are resistant to the drug can outcompete their susceptible neighbors, dominating the population. Counterintuitively, one can also co-opt this process to achieve the opposite result, ultimately defeating drug resistance. For example, a mutation that causes resistance to one drug may cause extreme susceptibility to another, a phenomenon known as collateral sensitivity.

"If that mutant is initially only a small fraction of the population, we can use the first drug to encourage its dominance, and then apply the second drug to rapidly wipe out the infection," said physician-scientist Jacob Scott, MD, DPhil, a practicing radiation oncologist at Cleveland Clinic and co-senior author on the study, referencing findings from a study his group published earlier this year. "But we also know that the first stage can be slow: mutations occur at random times, and waiting long enough until the mutant fully takes over could compromise treatment effectiveness and patient outcomes. The time it takes to ensure these interventions are successful has been a significant limitation to adopting evolutionary medicine into clinical practice."

Speeding up this process is where quantum physics can provide inspiration. "The randomness of mutations in evolution has intriguing mathematical parallels to the randomness of quantum phenomena," according to Prof. Michael Hinczewski, a theoretical biophysicist at Case Western Reserve University and co-senior author. "This randomness makes it challenging to reliably and quickly drive a quantum system from one state to another. Solving this driving problem is an essential ingredient in certain kinds of quantum computing. Our new study exploits these parallels, translating a particular quantum technique known as counterdiabatic driving into the language of evolutionary biology."

"Imagine trying to get a system to follow a desired path from an initial to a final state over a short time--whether this path is a sequence of quantum states or varying proportions of mutants in an evolving population," said Prof. Hinczewski. "Counterdiabatic driving is a form of dynamic correction, providing just enough external intervention to keep the system on the path at every instant no matter how fast the protocol."

The researchers created a mathematical algorithm to calculate this intervention in evolutionary medicine applications. The algorithm's output is a prescription for dynamically altering the drug dosages or types to stay on the target path. The team demonstrated their technique by using it to manipulate evolution in simulations of living cells. These simulations were based on experimental data from an earlier study on a set of mutants showing varying degrees of resistance to anti-malarial drugs.

Counterdiabatic driving changed the proportion of mutants, affecting the population's overall drug sensitivity, faster and with better control than could be expected using current experimental methods in evolutionary medicine.

Given the team's promising findings, the next phase of their research will be to conduct direct experimental testing of the approach. As the first example of counterdiabatic driving in a biological context, the researchers are hopeful that their work could provide a foundation for a novel area of study: quantum-inspired biological control. The researchers plan to apply these ideas to other biological systems that share similarities with evolution, such as stem cell development and ecology.

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Adapting ideas from quantum physics to calculate alternative interventions for infection and cancer - Science Codex

Global Degenerative Disc Disease Therapeutics Market Checkout the Unpredictable Future: Industry Applications, Competitors growth prospects, Industry…

Reportspedia published a new report, titled, Degenerative Disc Disease Therapeutics Market. GlobalDegenerative Disc Disease Therapeutics MarketPast, Present & Forecast Research 2020-2027 presents all-inclusive analysis & fundamental insights segmented by top companies, product type, geographical regions, applications & end-users. This brief breakdown provides 360-degree & complete Degenerative Disc Disease Therapeutics overview stating the opportunities, developmental factors, constraints & risks analysis. The forecast industry situations are presented based on past & present Smith Machines industry situations & growth rate.

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Samumed LLC DiscGenics Inc U.S. Stem Cell Inc BioRestorative Therapies Inc Biopharm GmbH AnGes Inc Bone Therapeutics SA Kolon TissueGene Inc Mesoblast Yuhan Corp Osiris Therapeutics Inc

This analysis includes a detailed share analysis of the key players. It also unveils the growth of the Degenerative Disc Disease Therapeutics Market participants along with their current statuses and key developments. The growth strategies employed by these players are also assessed in the report and are prognosticated to facilitate the study of the competitive landscape of the global Degenerative Disc Disease Therapeutics Market.

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ALLOB AMG-0101 BRTX-100 OTICR-01 Others

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Global Degenerative Disc Disease Therapeutics Market Checkout the Unpredictable Future: Industry Applications, Competitors growth prospects, Industry...

Review of Trials Currently Testing Stem Cells for Treatment of Respiratory Diseases: Facts Known to Date and Possible Applications to COVID-19 -…

This article was originally published here

Stem Cell Rev Rep. 2020 Aug 22. doi: 10.1007/s12015-020-10033-6. Online ahead of print.

ABSTRACT

Therapeutic clinical and preclinical studies using cultured cells are on the rise, especially now that the World Health Organization (WHO) declared coronavirus disease 2019 (COVID-19) a public health emergency of international concern, in January, 2020. Thus, this study aims to review the outcomes of ongoing clinical studies on stem cells in Severe Acute Respiratory Syndrome (SARS), Acute Respiratory Distress Syndrome (ARDS), and Middle East Respiratory Syndrome (MERS). The results will be associated with possible applications to COVID-19. Only three clinical trials related to stem cells are considered complete, whereby two are in Phase 1 and one is in Phase 2. Basically, the ongoing studies on coronavirus are using mesenchymal stem cells (MSCs) derived from bone marrow or the umbilical cord to demonstrate their feasibility, safety, and tolerability. The studies not related to coronavirus are all in ARDS conditions; four of them are in Phase 1 and three in Phase 2. With the COVID-19 boom, many clinical trials are being carried out using different sources with an emphasis on MSC-based therapy used to inhibit inflammation. One of the biggest challenges in the current treatment of COVID-19 is the cytokine storm, however MSCs can prevent or mitigate this cytokine storm through their immunomodulatory capacity. We look forward to the results of the ongoing clinical trials to find a treatment for the disease. Researchers around the world are joining forces to help fight COVID-19. Stem cells used in the current clinical studies are a new therapeutic promise for COVID-19 where pharmacological treatments seem insufficient.Graphical Abstract.

PMID:32827081 | DOI:10.1007/s12015-020-10033-6

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Review of Trials Currently Testing Stem Cells for Treatment of Respiratory Diseases: Facts Known to Date and Possible Applications to COVID-19 -...

Orchard Therapeutics Announces Clinical Data Presentations at the 46th Annual Meeting of the European Society for Blood and Marrow Transplantation…

BOSTON and LONDON, Aug. 24, 2020 (GLOBE NEWSWIRE) -- Orchard Therapeutics (Nasdaq: ORTX), a global gene therapy leader, today announced presentations at the upcoming 46th Annual Meeting of the European Society for Blood and Marrow Transplantation (EBMT), taking place virtually from August 29 - September 1, 2020. New interim data from OTL-203, an investigational gene therapy for the treatment of mucopolysaccharidosis type I (MPS-I), will be shared as part of an invited oral presentation titled Gene Therapy in Leucodystrophies and Other Metabolic Disorders.

The presentations are listed below and the full preliminary program is available online at the EBMT Annual Meeting website. Presentations will be available to registered attendees for virtual viewing throughout the duration of the live meeting and content will be accessible online following the close of the meeting.

Invited Oral Presentation Details

E7-2: Gene Therapy in Leucodystrophies and Other Metabolic Disorders Session: Gene Therapy for Inherited Disorders 2020 Presenter: M. Ester Bernardo, M.D., Ph.D., San Raffaele Telethon Institute for Gene Therapy (SR-Tiget), Italy Date and time: Monday, August 31, 2020, 4:50-5:10pm CET/10:50-11:10am ET

ePoster Details

Ex-vivo Autologous Haematopoietic Stem Cell Gene Therapy in Mucopolysaccharidosis Type IIIA* Poster Session & Number: Gene Therapy; ePoster A214

Lentiviral Hematopoietic Stem and Progenitor Cell Gene Therapy (HSPC-GT) For Metachromatic Leukodystrophy (MLD): Clinical Outcomes From 33 Patients Poster Session & Number: Gene Therapy; ePoster O075

About Orchard Orchard Therapeutics is a global gene therapy leader dedicated to transforming the lives of people affected by rare diseases through the development of innovative, potentially curative gene therapies. Our ex vivo autologous gene therapy approach harnesses the power of genetically modified blood stem cells and seeks to correct the underlying cause of disease in a single administration. In 2018, Orchard acquired GSKs rare disease gene therapy portfolio, which originated from a pioneering collaboration between GSK and the San Raffaele Telethon Institute for Gene Therapy in Milan, Italy. Orchard now has one of the deepest and most advanced gene therapy product candidate pipelines in the industry spanning multiple therapeutic areas where the disease burden on children, families and caregivers is immense and current treatment options are limited or do not exist.

Orchard has its global headquarters in London and U.S. headquarters in Boston. For more information, please visit http://www.orchard-tx.com, and follow us on Twitter and LinkedIn.

Availability of Other Information About Orchard Investors and others should note that Orchard communicates with its investors and the public using the company website (www.orchard-tx.com), the investor relations website (ir.orchard-tx.com), and on social media (Twitter and LinkedIn), including but not limited to investor presentations and investor fact sheets, U.S. Securities and Exchange Commission filings, press releases, public conference calls and webcasts. The information that Orchard posts on these channels and websites could be deemed to be material information. As a result, Orchard encourages investors, the media, and others interested in Orchard to review the information that is posted on these channels, including the investor relations website, on a regular basis. This list of channels may be updated from time to time on Orchards investor relations website and may include additional social media channels. The contents of Orchards website or these channels, or any other website that may be accessed from its website or these channels, shall not be deemed incorporated by reference in any filing under the Securities Act of 1933.

Forward-Looking Statements This press release contains certain forward-looking statements about Orchards strategy, future plans and prospects, which are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include express or implied statements relating to, among other things, Orchards business strategy and goals, and the therapeutic potential of Orchards product candidates, including the product candidate or candidates referred to in this release. These statements are neither promises nor guarantees and are subject to a variety of risks and uncertainties, many of which are beyond Orchards control, which could cause actual results to differ materially from those contemplated in these forward-looking statements. In particular, these risks and uncertainties include, without limitation: the severity of the impact of the COVID-19 pandemic on Orchards business, including on clinical development and commercial programs; the risk that any one or more of Orchards product candidates, including the product candidate or candidates referred to in this release, will not be approved, successfully developed or commercialized; the risk of cessation or delay of any of Orchards ongoing or planned clinical trials; the risk that Orchard may not successfully recruit or enroll a sufficient number of patients for its clinical trials; the risk that prior results, such as signals of safety, activity or durability of effect, observed from preclinical studies or clinical trials will not be replicated or will not continue in ongoing or future studies or trials involving Orchards product candidates; the delay of any of Orchards regulatory submissions; the failure to obtain marketing approval from the applicable regulatory authorities for any of Orchards product candidates or the receipt of restricted marketing approvals; and the risk of delays in Orchards ability to commercialize its product candidates, if approved. Given these uncertainties, the reader is advised not to place any undue reliance on such forward-looking statements.

Other risks and uncertainties faced by Orchard include those identified under the heading "Risk Factors" in Orchards quarterly report on Form 10-Q for the quarter ended June 30, 2020, as filed with the U.S. Securities and Exchange Commission (SEC), as well as subsequent filings and reports filed with the SEC. The forward-looking statements contained in this press release reflect Orchards views as of the date hereof, and Orchard does not assume and specifically disclaims any obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as may be required by law.

*Patient was treated by the Royal Manchester Childrens Hospital (RMCH) under a Specials license, granted by the UK government for the use of an unlicensed pharmaceutical product in situations of high unmet need when there is no other treatment option available. Orchard holds the license to the MPS-IIIA investigational gene therapy product (OTL-201) and is funding the ongoing proof-of-concept clinical trial being conducted at RMCH, which utilizes the same technology and procedures that were used to treat this first MPS-IIIA patient.

Contacts

Investors Renee Leck Director, Investor Relations +1 862-242-0764 Renee.Leck@orchard-tx.com

Media Molly Cameron Manager, Corporate Communications +1 978-339-3378 media@orchard-tx.com

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Orchard Therapeutics Announces Clinical Data Presentations at the 46th Annual Meeting of the European Society for Blood and Marrow Transplantation...

Second ASCT Has a Role in Relapsed Multiple Myeloma After First Transplant – Cancer Therapy Advisor

The landscape of treatment for relapsed multiple myeloma has evolved in recent years. Second salvage autologous hematopoietic stem cell transplantation (AHCT) remains an option in these patients, but its use varies widely, according to a recently published letter to the editor.

Choosing therapy in relapsed multiple myeloma is becoming increasingly complex in the crowded space of emerging and existing therapies, the researchers wrote.

To assess the use of second AHCT, researchers from the Medical College of Wisconsin and the University of Arkansas examined outcomes of 975 patients who underwent second transplant between 2010 and 2015 in the United States and Canada after relapse following first transplant.

With a median follow-up of 38 months, the rate of nonrelapse mortality was 1% at day 100, 1% at day 1 year, and 2% at 3 years. Cumulative incidence of relapse/progression at 1 year was 49%, increasing to 84% at 3 years.

Those patients who relapsed 3 years or later after first transplant had significantly lower incidence of relapse or progression after second transplant compared with those patients who relapsed between 24 and 35 months after first transplant (P =.02).

Additionally, those patients who relapsed 3 years or later after first transplant had significantly better progression-free (P =.01) and overall survival (P =.02) compared with those who relapsed earlier.

Disease status prior to second transplant was prognostic for relapse/progression, progression-free survival, and overall survival. Those patients who achieved very good partial response or better prior to second transplant had lower risk for relapse/progression and better progression-free survival compared with patients with partial response or stable disease.

The outcomes reported in our study are comparable with some of the new approved FDA regimens in that space, the researchers wrote.

Reference

Dhakal B, DSouza A, Kleman A, et al. Salvage second transplantation in relapsed multiple myeloma. Leukemia. Published August 4, 2020. doi:10.1038/s41375-020-1005-8

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Second ASCT Has a Role in Relapsed Multiple Myeloma After First Transplant - Cancer Therapy Advisor

McCloskey Explores Merits of Targeted Treatments and HMAs in MDS – Targeted Oncology

The options for targeted therapy and treatment with hypomethylating agents was discussed during a virtual Case Based Peer Perspectives event, which highlighted the case of a 75-year-old male patient with myelodysplastic syndromes (MDS). The discussion was led by James K. McCloskey II, MD, a medical oncologist, Division of Leukemia, Adult Blood and Marrow Stem Cell Transplantation Program, John Theurer Cancer Center, at Hackensack Meridian Health.

Targeted Oncology: What are the treatment regimens for the patient who isnt a candidate for induction therapy, according to the National Comprehensive Cancer Network (NCCN) guidelines?

MCCLOSKEY: For patients who are not candidates for induction therapy, the NCCN suggests venetoclax [Venclexta] in combination with HMA [hypomethylating agents] or LDAC [cladribine plus low-dose cytarabine], HMA alone, glasdegib [Daurismo] in combination with LDAC, LDAC alone, and Mylotarg [gemtuzumab ozogamicin].

What was the rationale for developing the liposomal combination of daunorubicin and cytarabine (Vyxeos) for this patient population?

This is a liposomal formulation of daunorubicin and cytarabine. I think the take-home point [regarding] the design of the drug is that the mechanism of action does not promote less toxicity but more effectiveness.

In preclinical models, we [found] that if we can administer anthracycline and cytarabine specifically in a 1:5 ratio, this is when we get the most potent antileukemic effect. The drug was designed to deliver that ratio and maintain that ratio in circulation.

The drug was approved based on a phase 3 randomized study [NCT01696084] that evaluated newly diagnosed patients with either treatment-related or secondary AML. These were patients between the ages of 60 and 75. The patients were deemed fit for intensive therapy, so their ECOG performance status was 0 to 2.

For this case, the patients cardiac events are concerning, although we dont know the circumstances under which he underwent stent placement. Otherwise, hes fitting into this category of patient. He specifically had MDS with prior HMA exposure. Hes 75, [which is] the upper age limit for patients in the study.

In this phase 3 trial, patients were randomized into treatment either with CPX-351 [n = 153] or 7 + 3 [n = 156]. They then were followed for treatment response. The patients who achieved a remission at any point and were eligible for transplant proceeded to transplant. Patients who failed to respond could receive salvage therapy. And those patients who achieved a response could go on to consolidation. At any point during the trial, patients could proceed to transplant.

An important consideration is that patients did not receive HiDAC [high-dose cytarabine] consolidation. They received 5 + 2, which is a European approach to treatment.

The FDA recommended the dosing description for the agent be 44 mg of daunorubicin and 100 mg/m of cytarabine. This formulation emphasizes the presence of the anthracycline.

What was the approval of this regimen based on?

The drug was approved based on overall survival data and investigators reported improved CR [complete response] rates. In the trial, 37% of patients experienced CR in the Vyxeos arm compared with 25% of patients in the control arm. If you consider CRis [complete remission with incomplete hematologic recovery], thats 47% for the Vyxeos arm compared with 33% for the control arm.

This did result in improved overall survival. Overall survival in the Vyxeos arm was 9.56 months compared with 5.95 months in the standard of care arm 7 + 3 [HR, 0.69; P = .003]. Patients who were treated with Vyxeos achieved the survival benefit whether they were in the older age group, between 70 and 75, or patients under the age of 75. Even those older patients did receive the survival benefit.

How does this affect consolidation and transplant?

If we follow the data out, it appears that Vyxeos improved outcomes both during consolidation with chemotherapy but also with patients who proceeded to stem cell transplant.

I think its important to note that this is post hoc analysis of the data, so these werent predefined groups. They were biased by the fact that these are responders.

Survival for patients who underwent consolidation with Vyxeos was 25 months compared with 8.5 months for 5 + 2. As we start to look at those patients who responded, we really see a significant benefit there. Looking at the impact [of Vyxeos] on transplant, among the patients who had a transplant, investigators reported more success getting folks to transplant in the Vyxeos arm: 49 patients in the Vyxeos arm compared with 32 patients in the control arm.

For patients who went to transplant in remission, it didnt matter which treatment regimen they received. The patients who received Vyxeos appeared to do better, with a median overall survival of 24 months compared with 12 months.

How does the safety profile of Vyxeos compare with standard induction?

I think most of the toxicities reported with Vyxeos are similar to what we expect to see with induction. In fact, the toxicities across the board are comparable, with no significant difference in cardiac toxicity and similar rates of infectious complications despite a delayed count recovery.

As you know, Vyxeos does often come with the downside of having delayed count recovery, but interestingly, we did not see increased risk of death from infection during that time. In terms of serious adverse effects, these 2 regimens are similar.

How was the dose for venetoclax determined?

The phase 1 study [NCT02203773] led by Dr DiNardo and colleagues evaluated venetoclax up to 800 mg in combination with both decitabine and Vidaza [azacitidine]. Its important to note that all the patients in the trial were HMA nave.

We did recently receive notice that the phase 3 data, published in Blood, which evaluated venetoclax plus azacitidine versus azacitidine alone, did meet its primary end point. What was striking was the remarkable response rate. For the elderly patient population who are unfit for transplant, the CR and CRi rates were 60% or 70%.

In terms of toxicity, there were few grade 3 and 4 toxicities, and not as many issues as we saw with the induction therapy that I previously mentioned.

But there were some concerns: 32% rate of febrile neutropenia, 12% pneumonia, 10% bacteremia. These occurred in a patient population that was less fit than the folks we just discussed and a little older in general.

What treatment options are available for patients with AML and high-risk MDS?

You might consider glasdegib, which we evaluated in clinical trials. We have used this in limited numbers of patients following the drugs approval.

If youre not familiar with glasdegib, its an inhibitor of the hedgehog pathway that targets the leukemia stem cell. It was studied in the BRIGHT study [NCT01546038]. This was a phase 2 randomized trial of patients with AML and high-risk MDS. Patients were randomized to either LDAC alone or LDAC in combination with glasdegib in a 2-to-1 fashion.d in the BRIGHT study [NCT01546038]. This was a phase 2 randomized trial of patients with AML and high-risk MDS. Patients were randomized to either LDAC alone or LDAC in combination with glasdegib in a 2-to-1 fashion.

The trial did include patients who had prior exposure to HMAs and, in fact, a substantial portion of these patients had been treated previously with HMA. The drug was approved based on the survival data around the same time as venetoclax. So glasdegib plus LDAC yielded an 8.8 months overall survival compared with LDAC alone for 4.9 months. I think as you start to get into the nitty-gritty of things, now that we have a lot of options in AML, there was a difference in response based on cytogenetic risk stratification.

Patients with good and intermediate risk exhibited a more significant response, a better improvement in overall survival, 12 months compared with 4.8 months in the LDAC arm [HR, 0.427; 80% CI, 0.300-0.609; P = .0008]. Patients with high-risk MDS and AML had a blunted response. Median OS for glasdegib was 4.7 months compared with 4.9 months for LDAC arm [HR, 0.633; 80% CI, 0.430-0.934; P = .0640].

The response data for glasdegib were not as impressive compared with venetoclax responses that I discussed earlier. The investigators reported a CR rate of 17% and CRi rate of 6.5%. They reported an overall response rate of 26% compared with 5% for LDAC alone. And I think that this is a good point to consider as we look at new agents for AML. Its always a point of conversation, especially in these older, more frail patients. How do we consider both a survival benefit and CR rate in a more elderly patient? If they could live with their disease and be relatively symptom-free, how important is that CR?

For this patient, is HMA still a consideration?

The patient was treated with venetoclax in combination with azacitidine. If the investigators followed the clinical trial regimen, this patient would not have been eligible for HMA.

But I think certainly, like many, depending on the patient and how much HMA they have received, we might consider still using HMA in combination with venetoclax as a salvage therapy. And the patient does have a response with a remission and is transfusion independent after 45 days on treatment.

Would you consider a bone marrow transplant for him?

We tend to use bone marrow transplants quite frequently, I think, because in our experience, almost all of these patients have very serious cytopenias eventually. We have found it helpful to do bone marrow transplants to document a response. However, if you have a patient who is doing great [and] the counts are beautiful, then maybe not.

Maybe that bone marrow transplant is not as helpful if the patient has had a full hematologic response. In general, our experience has been that many of these patients, especially like this patient were discussing, theyre likely to end up cytopenic at the end of their first cycle of treatment. And so then were left really scratching our heads. Are they cytopenic because there is disease in the bone marrow? Or are they cytopenic because theyre aplastic?

References:

1. NCCN Clinical Practice Guidelines in Oncology. Acute myeloid leukemia, version 3.2020. NCCN. Accessed July 29, 2020. https://bit.ly/3jSYRs3

2. Lancet JE, Uy Gl, Cortes JE, et al. Final results of a phase III randomized trial of CPX-351 versus 7+3 in older patients with newly diagnosed high risk (secondary) AML. J Clin Oncol. 2016;34(suppl 15):7000. doi: 10.1200/JCO.2016.34.15_suppl.7000

3. Kolitz JE, Strickland SA, Cortes JE, et al. Consolidation outcomes in CPX-351 versus cytarabine/daunorubicin-treated older patients with high-risk/secondary acute myeloid leukemia. Leuk Lymphoma. 2020;61(3):631-640. doi:10.1080/10428194.2019.1688320

4. Dinardo CD, Pratz KW, Potluri J, et al. Durable response with venetoclax in combination with decitabine or azacitidine in elderly patients with acute myeloid leukemia (AML). J Clin Oncol. 2018;36(suppl 15):7010. doi:10.1200/JCO.2018.36.15_suppl.7010

5. DiNardo CD, Pratz K, Pullarkat V, et al. Venetoclax combined with decitabine or azacitidine in treatment-naive, elderly patients with acute myeloid leukemia. Blood. 2019;133(1):7-17. doi:10.1182/blood-2018-08-868752

6. Cortes JE, Heidel FH, Hellmann A, et al. Randomized comparison of low dose cytarabine with or without glasdegib in patients with newly diagnosed acute myeloid leukemiaor high-risk m yelodysplastic syndrome. Leukemia. 2019;33(2):379-389. doi:10.1038/s41375-018-0312-9

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McCloskey Explores Merits of Targeted Treatments and HMAs in MDS - Targeted Oncology

Allogeneic Stem Cell Therapy Market Study for 2020 to 2026 Providing Information on Key Players, Growth Drivers and Industry Challenges|Escape…

Allogeneic Stem Cell Therapy Market Los Angeles, United State- The global Allogeneic Stem Cell Therapy market is carefully researched in the report while largely concentrating on top players and their business tactics, geographical expansion, market segments, competitive landscape, manufacturing, and pricing and cost structures. Each section of the research study is specially prepared to explore key aspects of the global Allogeneic Stem Cell Therapy market. For instance, the market dynamics section digs deep into the drivers, restraints, trends, and opportunities of the global Allogeneic Stem Cell Therapy Market. With qualitative and quantitative analysis, we help you with thorough and comprehensive research on the global Allogeneic Stem Cell Therapy market. We have also focused on SWOT, PESTLE, and Porters Five Forces analyses of the global Allogeneic Stem Cell Therapy market.

Leading players of the global Allogeneic Stem Cell Therapy market are analyzed taking into account their market share, recent developments, new product launches, partnerships, mergers or acquisitions, and markets served. We also provide an exhaustive analysis of their product portfolios to explore the products and applications they concentrate on when operating in the global Allogeneic Stem Cell Therapy market. Furthermore, the report offers two separate market forecasts one for the production side and another for the consumption side of the global Allogeneic Stem Cell Therapy market. It also provides useful recommendations for new as well as established players of the global Allogeneic Stem Cell Therapy market.

Get PDF template of this report: https://www.qyresearch.com/sample-form/form/2043756/global-and-china-allogeneic-stem-cell-therapy-market

Allogeneic Stem Cell Therapy Market Leading Players

, Escape Therapeutics, Inc., Lonza Group Ltd., Osiris Therapeutics (Smith & Nephew), NuVasive, Chiesi Pharmaceuticals, JCR Pharmaceutical, Pharmicell, Anterogen, MolMed S.p.A., Takeda (TiGenix)

Allogeneic Stem Cell Therapy Segmentation by Product

, Adult Stem Cell Therapy, Human Embryonic Stem Cell Therapy, Induced Pluripotent Stem Cell Therapy, Others Allogeneic Stem Cell Therapy

Allogeneic Stem Cell Therapy Segmentation by Application

Musculoskeletal Disorder, Wounds & Injuries, Cardiovascular Diseases, Others

Report Objectives

Analyzing the size of the global Allogeneic Stem Cell Therapy market on the basis of value and volume.

Accurately calculating the market shares, consumption, and other vital factors of different segments of the global Allogeneic Stem Cell Therapy market.

Exploring the key dynamics of the global Allogeneic Stem Cell Therapy market.

Highlighting important trends of the global Allogeneic Stem Cell Therapy market in terms of production, revenue, and sales.

Deeply profiling top players of the global Allogeneic Stem Cell Therapy market and showing how they compete in the industry.

Studying manufacturing processes and costs, product pricing, and various trends related to them.

Showing the performance of different regions and countries in the global Allogeneic Stem Cell Therapy market.

Forecasting the market size and share of all segments, regions, and the global market.

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Table of Contents.

1 Report Overview 1.1 Study Scope 1.2 Market Analysis by Type 1.2.1 Global Allogeneic Stem Cell Therapy Market Size Growth Rate by Type: 2020 VS 2026 1.2.2 Adult Stem Cell Therapy 1.2.3 Human Embryonic Stem Cell Therapy 1.2.4 Induced Pluripotent Stem Cell Therapy 1.2.5 Others 1.3 Market by Application 1.3.1 Global Allogeneic Stem Cell Therapy Market Share by Application: 2020 VS 2026 1.3.2 Musculoskeletal Disorder 1.3.3 Wounds & Injuries 1.3.4 Cardiovascular Diseases 1.3.5 Others 1.4 Study Objectives 1.5 Years Considered 2 Global Growth Trends 2.1 Global Allogeneic Stem Cell Therapy Market Perspective (2015-2026) 2.2 Global Allogeneic Stem Cell Therapy Growth Trends by Regions 2.2.1 Allogeneic Stem Cell Therapy Market Size by Regions: 2015 VS 2020 VS 2026 2.2.2 Allogeneic Stem Cell Therapy Historic Market Share by Regions (2015-2020) 2.2.3 Allogeneic Stem Cell Therapy Forecasted Market Size by Regions (2021-2026) 2.3 Industry Trends and Growth Strategy 2.3.1 Market Trends 2.3.2 Market Drivers 2.3.3 Market Challenges 2.3.4 Market Restraints 3 Competition Landscape by Key Players 3.1 Global Top Allogeneic Stem Cell Therapy Players by Market Size 3.1.1 Global Top Allogeneic Stem Cell Therapy Players by Revenue (2015-2020) 3.1.2 Global Allogeneic Stem Cell Therapy Revenue Market Share by Players (2015-2020) 3.2 Global Allogeneic Stem Cell Therapy Market Share by Company Type (Tier 1, Tier 2 and Tier 3) 3.3 Players Covered: Ranking by Allogeneic Stem Cell Therapy Revenue 3.4 Global Allogeneic Stem Cell Therapy Market Concentration Ratio 3.4.1 Global Allogeneic Stem Cell Therapy Market Concentration Ratio (CR5 and HHI) 3.4.2 Global Top 10 and Top 5 Companies by Allogeneic Stem Cell Therapy Revenue in 2019 3.5 Key Players Allogeneic Stem Cell Therapy Area Served 3.6 Key Players Allogeneic Stem Cell Therapy Product Solution and Service 3.7 Date of Enter into Allogeneic Stem Cell Therapy Market 3.8 Mergers & Acquisitions, Expansion Plans 4 Allogeneic Stem Cell Therapy Breakdown Data by Type (2015-2026) 4.1 Global Allogeneic Stem Cell Therapy Historic Market Size by Type (2015-2020) 4.2 Global Allogeneic Stem Cell Therapy Forecasted Market Size by Type (2021-2026) 5 Allogeneic Stem Cell Therapy Breakdown Data by Application (2015-2026) 5.1 Global Allogeneic Stem Cell Therapy Historic Market Size by Application (2015-2020) 5.2 Global Allogeneic Stem Cell Therapy Forecasted Market Size by Application (2021-2026) 6 North America 6.1 North America Allogeneic Stem Cell Therapy Market Size (2015-2026) 6.2 North America Allogeneic Stem Cell Therapy Market Size by Type (2015-2020) 6.3 North America Allogeneic Stem Cell Therapy Market Size by Application (2015-2020) 6.4 North America Allogeneic Stem Cell Therapy Market Size by Country (2015-2020) 6.4.1 United States 6.4.2 Canada 7 Europe 7.1 Europe Allogeneic Stem Cell Therapy Market Size (2015-2026) 7.2 Europe Allogeneic Stem Cell Therapy Market Size by Type (2015-2020) 7.3 Europe Allogeneic Stem Cell Therapy Market Size by Application (2015-2020) 7.4 Europe Allogeneic Stem Cell Therapy Market Size by Country (2015-2020) 7.4.1 Germany 7.4.2 France 7.4.3 U.K. 7.4.4 Italy 7.4.5 Russia 7.4.6 Nordic 7.4.7 Rest of Europe 8 China 8.1 China Allogeneic Stem Cell Therapy Market Size (2015-2026) 8.2 China Allogeneic Stem Cell Therapy Market Size by Type (2015-2020) 8.3 China Allogeneic Stem Cell Therapy Market Size by Application (2015-2020) 8.4 China Allogeneic Stem Cell Therapy Market Size by Region (2015-2020) 8.4.1 China 8.4.2 Japan 8.4.3 South Korea 8.4.4 Southeast Asia 8.4.5 India 8.4.6 Australia 8.4.7 Rest of Asia-Pacific 9 Japan 9.1 Japan Allogeneic Stem Cell Therapy Market Size (2015-2026) 9.2 Japan Allogeneic Stem Cell Therapy Market Size by Type (2015-2020) 9.3 Japan Allogeneic Stem Cell Therapy Market Size by Application (2015-2020) 9.4 Japan Allogeneic Stem Cell Therapy Market Size by Country (2015-2020) 9.4.1 Mexico 9.4.2 Brazil 10 South Korea 10.1 South Korea Allogeneic Stem Cell Therapy Market Size (2015-2026) 10.2 South Korea Allogeneic Stem Cell Therapy Market Size by Type (2015-2020) 10.3 South Korea Allogeneic Stem Cell Therapy Market Size by Application (2015-2020) 10.4 South Korea Allogeneic Stem Cell Therapy Market Size by Country (2015-2020) 10.4.1 Turkey 10.4.2 Saudi Arabia 10.4.3 UAE 10.4.4 Rest of Middle East & Africa 11 Key Players Profiles 11.1 Escape Therapeutics, Inc. 11.1.1 Escape Therapeutics, Inc. Company Details 11.1.2 Escape Therapeutics, Inc. Business Overview 11.1.3 Escape Therapeutics, Inc. Allogeneic Stem Cell Therapy Introduction 11.1.4 Escape Therapeutics, Inc. Revenue in Allogeneic Stem Cell Therapy Business (2015-2020)) 11.1.5 Escape Therapeutics, Inc. Recent Development 11.2 Lonza Group Ltd. 11.2.1 Lonza Group Ltd. Company Details 11.2.2 Lonza Group Ltd. Business Overview 11.2.3 Lonza Group Ltd. Allogeneic Stem Cell Therapy Introduction 11.2.4 Lonza Group Ltd. Revenue in Allogeneic Stem Cell Therapy Business (2015-2020) 11.2.5 Lonza Group Ltd. Recent Development 11.3 Osiris Therapeutics (Smith & Nephew) 11.3.1 Osiris Therapeutics (Smith & Nephew) Company Details 11.3.2 Osiris Therapeutics (Smith & Nephew) Business Overview 11.3.3 Osiris Therapeutics (Smith & Nephew) Allogeneic Stem Cell Therapy Introduction 11.3.4 Osiris Therapeutics (Smith & Nephew) Revenue in Allogeneic Stem Cell Therapy Business (2015-2020) 11.3.5 Osiris Therapeutics (Smith & Nephew) Recent Development 11.4 NuVasive 11.4.1 NuVasive Company Details 11.4.2 NuVasive Business Overview 11.4.3 NuVasive Allogeneic Stem Cell Therapy Introduction 11.4.4 NuVasive Revenue in Allogeneic Stem Cell Therapy Business (2015-2020) 11.4.5 NuVasive Recent Development 11.5 Chiesi Pharmaceuticals 11.5.1 Chiesi Pharmaceuticals Company Details 11.5.2 Chiesi Pharmaceuticals Business Overview 11.5.3 Chiesi Pharmaceuticals Allogeneic Stem Cell Therapy Introduction 11.5.4 Chiesi Pharmaceuticals Revenue in Allogeneic Stem Cell Therapy Business (2015-2020) 11.5.5 Chiesi Pharmaceuticals Recent Development 11.6 JCR Pharmaceutical 11.6.1 JCR Pharmaceutical Company Details 11.6.2 JCR Pharmaceutical Business Overview 11.6.3 JCR Pharmaceutical Allogeneic Stem Cell Therapy Introduction 11.6.4 JCR Pharmaceutical Revenue in Allogeneic Stem Cell Therapy Business (2015-2020) 11.6.5 JCR Pharmaceutical Recent Development 11.7 Pharmicell 11.7.1 Pharmicell Company Details 11.7.2 Pharmicell Business Overview 11.7.3 Pharmicell Allogeneic Stem Cell Therapy Introduction 11.7.4 Pharmicell Revenue in Allogeneic Stem Cell Therapy Business (2015-2020) 11.7.5 Pharmicell Recent Development 11.8 Anterogen 11.8.1 Anterogen Company Details 11.8.2 Anterogen Business Overview 11.8.3 Anterogen Allogeneic Stem Cell Therapy Introduction 11.8.4 Anterogen Revenue in Allogeneic Stem Cell Therapy Business (2015-2020) 11.8.5 Anterogen Recent Development 11.9 MolMed S.p.A. 11.9.1 MolMed S.p.A. Company Details 11.9.2 MolMed S.p.A. Business Overview 11.9.3 MolMed S.p.A. Allogeneic Stem Cell Therapy Introduction 11.9.4 MolMed S.p.A. Revenue in Allogeneic Stem Cell Therapy Business (2015-2020) 11.9.5 MolMed S.p.A. Recent Development 11.10 Takeda (TiGenix) 11.10.1 Takeda (TiGenix) Company Details 11.10.2 Takeda (TiGenix) Business Overview 11.10.3 Takeda (TiGenix) Allogeneic Stem Cell Therapy Introduction 11.10.4 Takeda (TiGenix) Revenue in Allogeneic Stem Cell Therapy Business (2015-2020) 11.10.5 Takeda (TiGenix) Recent Development 12 Analysts Viewpoints/Conclusions 13 Appendix 13.1 Research Methodology 13.1.1 Methodology/Research Approach 13.1.2 Data Source 13.2 Disclaimer 13.3 Author Details

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Allogeneic Stem Cell Therapy Market Study for 2020 to 2026 Providing Information on Key Players, Growth Drivers and Industry Challenges|Escape...

NantKwest and ImmunityBio Sign Collaboration Agreement for Joint Development, Manufacturing, Marketing, and Commercialization of COVID-19 Vaccine and…

EL SEGUNDO, Calif. & CULVER CITY, Calif.--(BUSINESS WIRE)--NantKwest, Inc. (Nasdaq: NK), a clinical-stage, natural killer cell-based therapeutics company, and ImmunityBio, a privately held immunotherapy company, today announced the signing of a definitive agreement to jointly develop, manufacture, market, and commercialize therapeutics and vaccines for combating the COVID-19 pandemic.

Under the terms of the definitive agreement, the two companies agree to share equally the costs incurred after August 21, 2020 of development, manufacturing, marketing, and commercialization of the products each is developing related to COVID-19. Should a product be commercialized successfully, the companies have agreed to a 60-40 percentage split of net profits, with the larger share going to the company that developed the product. The agreement also details the structure of shared governance of the joint collaboration.

The two product candidates currently in development under the agreement are a mesenchymal stem cell (MSC) therapeutic from NantKwest, whose goal is to reduce the time a critically ill patient spends on a ventilator; and a COVID-19 vaccine product from ImmunityBio, which is anticipated to soon enter into a phase I clinical trial.

The severity and global nature of the COVID-19 pandemic demands that researchers move rapidly and have the resources necessary to develop ways to fight this deadly virus, said Patrick Soon-Shiong, Chairman and CEO of NantKwest and ImmunityBio. The agreement strengthens the efforts of both companies on behalf of patients, while also ensuring each company will earn a fair share of the returns of a successful product.

About NantKwest

NantKwest (NASDAQ: NK) is an innovative, clinical-stage immunotherapy company focused on harnessing the power of the innate immune system to treat cancer and infectious diseases. NantKwest is the leading producer of clinical dose forms of off-the-shelf natural killer (NK) cell therapies. The activated NK cell platform is designed to destroy cancer and virally-infected cells. The safety of these optimized, activated NK cellsas well as their activity against a broad range of cancershas been tested in phase I clinical trials in Canada and Europe, as well as in multiple phase I and II clinical trials in the United States. By leveraging an integrated and extensive genomics and transcriptomics discovery and development engine, together with a pipeline of multiple, clinical-stage, immuno-oncology programs, NantKwests goal is to transform medicine by bringing novel NK cell-based therapies to routine clinical care. NantKwest is a member of the NantWorks ecosystem of companies. For more information, please visit http://www.nantkwest.com

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include statements concerning or implying that NantKwest will be successful in improving the treatment of cancer or other critical illnesses, including COVID-19. Risks and uncertainties related to these endeavors include, but are not limited to, obtaining FDA approval of NantKwests NK cells and MSC as well as other therapeutics and manufacturing challenges.

Forward-looking statements are based on managements current expectations and are subject to various risks and uncertainties that could cause actual results to differ materially and adversely from those expressed or implied by such forward-looking statements. Accordingly, these forward-looking statements do not constitute guarantees of future performance, and you are cautioned not to place undue reliance on these forward-looking statements.

These and other risks regarding NantKwests business are described in detail in its Securities and Exchange Commission filings, including in NantKwests Quarterly Report on Form 10-Q for the quarter ended June 30, 2020. These forward-looking statements speak only as of the date hereof, and we disclaim any obligation to update these statements except as may be required by law.

About ImmunityBio

ImmunityBio, Inc. is a late-clinical-stage immunotherapy company developing next-generation therapies that drive immunogenic mechanisms for defeating cancers and infectious disease. The companys immunotherapy platform activates both the innate (natural killer cell and macrophage) and adaptive (T cell) immune systems to create long-term immunological memory. This novel approach is designed to eliminate the need for high-dose chemotherapy, improve upon the outcomes of current CAR T-cell therapies, and extend beyond checkpoint inhibitors.

ImmunityBios platform is based on the foundation of three separate modalities: antibody cytokine fusion proteins, synthetic immunomodulators, and second-generation vaccine technologies.

ImmunityBios lead cytokine infusion protein, a novel interleukin-15 (IL-15) superagonist complex (Anktiva), has received Breakthrough Therapy and Fast Track Designations from the U.S. Food and Drug Administration (FDA) for BCG-unresponsive CIS non-muscle invasive bladder cancer (NMIBC). Other indications currently at registration-stage trials include BCG-unresponsive papillary bladder cancer, first and second line lung cancer, triple-negative breast cancer, metastatic pancreatic cancer, recurrent glioblastoma, and soft tissue sarcoma in combination with the companys synthetic immune modulator (Aldoxorubicin).

ImmunityBio is also developing therapies, including vaccines, for the prevention and treatment of HIV, influenza, and the coronavirus SARS-CoV-2 with its second-generation human adenovirus (hAd5) vaccine platform.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include statements concerning or implying that ImmunityBio will be successful in improving the treatment of various diseases, including, but not limited to the novel coronavirus and cancer. Risks and uncertainties related to this endeavor include, but are not limited to, the companys beliefs regarding the success, cost, and timing of its development activities and clinical trials.

Forward-looking statements are based on managements current expectations and are subject to various risks and uncertainties that could cause actual results to differ materially and adversely from those expressed or implied by such forward-looking statements. Accordingly, these forward-looking statements do not constitute guarantees of future performance, and you are cautioned not to place undue reliance on these forward-looking statements. These forward-looking statements speak only as of the date hereof, and we disclaim any obligation to update these statements except as may be required by law.

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NantKwest and ImmunityBio Sign Collaboration Agreement for Joint Development, Manufacturing, Marketing, and Commercialization of COVID-19 Vaccine and...

Could gene therapy stem the damage of Parkinson’s? – Health24

It may be possible to protect Parkinson's patients' brains from further damage by turning off a "master regulator" gene, researchers report.

"One of the biggest challenges in treating Parkinson's, other than the lack of therapies that impede disease progression, is that the disease has already laid waste to significant portions of the brain by the time it is diagnosed," said researcher Viviane Labrie, an associate professor at the Van Andel Institute, in Grand Rapids, Michigan.

"If we can find a way to protect critical brain cells from Parkinson's-related damage early on, we could potentially delay or even prevent symptom onset," she suggested in an institute news release.

Deadly for brain cells

Labrie and her colleagues compared the brains of Parkinson's patients and people without the neurodegenerative disease and found that a master regulator gene called TET2 was overactive in the brains of those with Parkinson's. That resulted in a heightened immune response and reactivation of the cell cycle.

While restarting the cell cycle is normal for many types of cells, it's deadly for brain cells, the study authors explained.

The researchers also found that reducing TET2 activity in mouse brains protects brain cells from inflammatory damage and the resulting neurodegeneration seen in Parkinson's disease patients.

These and other findings suggest that lowering TET2 activity could provide a new way to preserve brain cells in Parkinson's patients, according to the authors of the study published in the journal Nature Neuroscience.

A complex disease

For example, reducing TET2 activity might be used after a patient has a major inflammatory event, such as an infection, to relieve residual inflammation without interfering with its normal, healthy role in the body.

"Parkinson's is a complex disease with a range of triggers. Temporarily reducing TET2 activity could be one way to interfere with multiple contributors to the disease, especially inflammatory events, and protect the brain from loss of dopamine-producing cells," Labrie said.

"More work is needed before a TET2-based intervention can be developed, but it is a new and a promising avenue that we already are exploring," she concluded.

Image credit: iStock

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Could gene therapy stem the damage of Parkinson's? - Health24