Sorrento Issues Update to its Previously Issued “FAQ” Regarding the Dividend of Scilex Holding Company Common Stock (Nasdaq: SCLX, “Scilex”)

SAN DIEGO, Feb. 17, 2023 (GLOBE NEWSWIRE) -- Sorrento Therapeutics, Inc. (Nasdaq: SRNE, “Sorrento”) today posted an update to its previously issued “Frequently Asked Questions” document under the “Investors” section of its website at www.sorrentotherapeutics.com regarding its recent dividend to Sorrento stockholders of shares of common stock of Scilex Holding Company previously held by Sorrento (the “Dividend Stock”).

Original post:
Sorrento Issues Update to its Previously Issued “FAQ” Regarding the Dividend of Scilex Holding Company Common Stock (Nasdaq: SCLX, “Scilex”)

Sutro Biopharma Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

SOUTH SAN FRANCISCO, Calif., Feb. 17, 2023 (GLOBE NEWSWIRE) -- Sutro Biopharma, Inc. (Sutro or the Company) (NASDAQ: STRO), a clinical-stage oncology company pioneering site-specific and novel-format antibody drug conjugates (ADCs), today announced that on February 15, 2023, the Compensation Committee of Sutro’s Board of Directors granted 90,000 shares of Sutro Biopharma stock options and 130,000 restricted stock units (RSUs) of Sutro common stock. These grants were made as an inducement material to the employees’ acceptance of employment with Sutro and were approved by the Compensation Committee of Sutro’s Board of Directors in accordance with Nasdaq Listing Rule 5635(c)(4).

View original post here:
Sutro Biopharma Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

TransCode Therapeutics Announces Closing of $1.5 Million Registered Direct Offering of Common Stock Priced At-The-Market under Nasdaq Rules

BOSTON, Feb. 17, 2023 (GLOBE NEWSWIRE) -- TransCode Therapeutics, Inc. (Nasdaq: RNAZ) (the “Company”), an RNA oncology company committed to more effectively treating cancer using RNA therapeutics, today announced the closing of its previously announced registered direct offering of 2,846,300 shares of common stock priced at-the-market under Nasdaq rules at $0.527 per share for gross proceeds of $1.5 million.

Original post:
TransCode Therapeutics Announces Closing of $1.5 Million Registered Direct Offering of Common Stock Priced At-The-Market under Nasdaq Rules

InMed Reports Second Quarter Fiscal 2023 Financial Results and Provides Business Update

VANCOUVER, British Columbia, Feb. 17, 2023 (GLOBE NEWSWIRE) -- InMed Pharmaceuticals Inc. (“InMed” or the “Company”) (Nasdaq: INM), a leader in the pharmaceutical research, development and manufacturing of rare cannabinoids and cannabinoid analogs, today announced financial results for the second quarter of fiscal year 2023 which ended December 31, 2022.

Read the original:
InMed Reports Second Quarter Fiscal 2023 Financial Results and Provides Business Update

Global Induced Pluripotent Stem Cell (iPSC) Industry Report 2023 …

DUBLIN, Feb. 13, 2023 /PRNewswire/ --The "Global Induced Pluripotent Stem Cell (iPSC) Industry Report - Market Size, Trends, and Forecasts, 2023" report has been added to ResearchAndMarkets.com's offering.

Since the discovery of induced pluripotent stem cell (iPSC) technology in 2006, significant progress has been made in stem cell biology and regenerative medicine. New pathological mechanisms have been identified and explained, new drugs identified by iPSC screens are in the pipeline, and the first clinical trials employing human iPSC-derived cell types have been initiated. iPSCs can be used to explore the causes of disease onset and progression, create and test new drugs and therapies, and treat previously incurable diseases.

Today, methods of commercializing induced pluripotent stem cells (iPSCs) include:

Since the discovery of iPSCs in 2006, it took only seven years for the first iPSC-derived cell product to be transplanted into a human patient in 2013. Since then, iPSC-derived cells have been used within a rapidly growing number of preclinical studies, physician-led studies, and clinical trials worldwide. There are also over 100 clinical trials underway that do not involve the transplant of iPSCs into humans, but rather, the creation and evaluation of iPSC lines for clinical purposes. Within these trials, iPSC lines are created from specific patient populations to determine if these cell lines could be a good model for a disease of interest.

2013 was a landmark year because it saw the first cellular therapy involving the transplant of iPSCs into humans initiated at the RIKEN Center in Kobe, Japan. Led by Dr. Masayo Takahashi, it investigated the safety of iPSC-derived cell sheets in patients with macular degeneration. In another world first, Cynata Therapeutics received approval in 2016 to launch the first formal clinical trial of an allogeneic iPSC-derived cell product (CYP-001) for the treatment of GvHD. CYP-001 is a iPSC-derived MSC product. In this historic trial, CYP-001 met its clinical endpoints and produced positive safety and efficacy data for the treatment of steroid-resistant acute GvHD.

Given this early success, Cynata is has advanced its iPSC-derived MSCs into Phase 2 trials for the severe complications associated with COVID-19, as well as GvHD and critical limb ischemia (CLI). It is also undertaking an impressive Phase 3 trial that will utilize Cynata's iPSC-derived MSC product, CYP-004, in 440 patients with osteoarthritis (OA). This trial represents the world's first Phase 3 clinical trial involving an iPSC-derived cell therapeutic product and the largest one ever completed. Not surprisingly, the Japanese behemoth FUJIFILM has been involved with the co-development and commercialization of Cynata's iPSC-derived MSCs through its 9% ownership stake in the company.

Many market competitors are also commercializing iPSC-derived products for use in drug development and discovery, disease modeling, and toxicology testing. Across the broader iPSC sector, FUJIFILM CDI (FCDI) is one of the largest and most dominant players. Cellular Dynamics International (CDI) was founded in 2004 by Dr. James Thomson at the University of Wisconsin-Madison, who in 2007 derived iPSC lines from human somatic cells for the first time. The feat was accomplished simultaneously by Dr. Shinya Yamanaka's lab in Japan. FUJIFILM acquired CDI in April 2015 for $307 million. Today, the combined company is the world's largest manufacturer of human cells created from iPSCs for use in research, drug discovery and regenerative medicine applications.

Another iPSC specialist is ReproCELL, a company that was established as a venture company originating from the University of Tokyo and Kyoto University in 2009. It became the first company worldwide to make iPSC products commercially available when it launched its ReproCardio product, which are human iPSC-derived cardiomyocytes. Within the European market, the dominant competitors are Evotec, Ncardia, and Axol Bioscience. Headquartered in Hamburg, Germany, Evotec is a drug discovery alliance and development partnership company. It is developing an iPSC platform with the goal to industrialize iPSC-based drug screening as it relates to throughput, reproducibility, and robustness. Today, Evotec's infrastructure represents one of the largest and most advanced iPSC platforms globally.

Ncardia was formed through the merger of Axiogenesis and Pluriomics in 2017. Its predecessor, Axiogenesis, was founded in 2011 with an initial focus on mouse embryonic stem cell-derived cells and assays. When Yamanaka's iPSC technology became available, Axiogenesis became the first European company to license it in 2010. Today, the combined company (Ncardia) is a global authority in cardiac and neural applications of human iPSCs. Founded in 2012, Axol Bioscience is a smaller but noteworthy competitor that specializes in iPSC-derived products. Headquartered in Cambridge, UK, it specializes in human cell culture, providing iPSC-derived cells and iPSC-specific cell culture products.

Of course, the world's largest research supply companies are also commercializing a diverse range of iPSC-derived products and services. Examples of these companies include Lonza, BD Biosciences, Thermo Fisher Scientific, Merck, Takara Bio, and countless others. In total, at least 80 market competitors now offer a diverse range of iPSC products, services, technologies, and therapeutics.

Key Topics Covered:

1. Report Overview

2. Introduction

3. Current Status of iPSC Industry

4. History of Induced Pluripotent Stem Cells (iPSCs)

5. Research Publications on iPSCs

6. iPSC: Patent Landscape Analysis

7. iPSC: Clinical Trial Landscape

8. Research Funding for iPSCs

9. M&A, Collaborations & Funding Activities in iPSC Sector

10. Generation of Induced Pluripotent Stem Cells: An Overview

11. Human iPSC Banking

12. Biomedical Applications of iPSCs

13. Market Overview

14. Company Profiles

Selection of Companies Mentioned

For more information about this report visit https://www.researchandmarkets.com/r/2q9nbt-induced?w=5

About ResearchAndMarkets.com ResearchAndMarkets.com is the world's leading source for international market research reports and market data. We provide you with the latest data on international and regional markets, key industries, the top companies, new products and the latest trends.

Media Contact:

Research and Markets Laura Wood, Senior Manager [emailprotected]

For E.S.T Office Hours Call +1-917-300-0470 For U.S./CAN Toll Free Call +1-800-526-8630 For GMT Office Hours Call +353-1-416-8900

U.S. Fax: 646-607-1904 Fax (outside U.S.): +353-1-481-1716

Logo: https://mma.prnewswire.com/media/539438/Research_and_Markets_Logo.jpg

SOURCE Research and Markets

Read more:
Global Induced Pluripotent Stem Cell (iPSC) Industry Report 2023 ...

Helocyte, Inc. Announces Positive Data from Stem Cell Transplant Donor Vaccination Trial to be presented at the 2023 Tandem Meetings, Transplantation…

Helocyte, Inc. Announces Positive Data from Stem Cell Transplant Donor Vaccination Trial to be presented at the 2023 Tandem Meetings, Transplantation and Cellular Therapy Meetings of ASTCT and CIBMTR  Marketscreener.com

More here:
Helocyte, Inc. Announces Positive Data from Stem Cell Transplant Donor Vaccination Trial to be presented at the 2023 Tandem Meetings, Transplantation...

Induced pluripotent stem cell technology: a decade of progress

Title & authors Abstract Conflict of interest statement Figures Similar articles Cited by Publication types MeSH terms Grant support LinkOut - more resources

Review

Affiliations Expand

Item in Clipboard

Review

Yanhong Shiet al. Nat Rev Drug Discov. 2017 Feb.

Display options

Format Abstract PubMed PMID

Item in Clipboard

Display options

Format Abstract PubMed PMID

Since the advent of induced pluripotent stem cell (iPSC) technology a decade ago, enormous progress has been made in stem cell biology and regenerative medicine. Human iPSCs have been widely used for disease modelling, drug discovery and cell therapy development. Novel pathological mechanisms have been elucidated, new drugs originating from iPSC screens are in the pipeline and the first clinical trial using human iPSC-derived products has been initiated. In particular, the combination of human iPSC technology with recent developments in gene editing and 3D organoids makes iPSC-based platforms even more powerful in each area of their application, including precision medicine. In this Review, we discuss the progress in applications of iPSC technology that are particularly relevant to drug discovery and regenerative medicine, and consider the remaining challenges and the emerging opportunities in the field.

Conflict of Interest

J.C.W. is a co-founder of Stem Cell Theranostics. S.Y. is a scientific advisor of iPS Academia Japan without salary. The other authors declare no conflict of interest.

Figure 1

A schematic for human iPSC-based

Figure 1

A schematic for human iPSC-based disease modeling. Human iPSCs are derived from individual

A schematic for human iPSC-based disease modeling. Human iPSCs are derived from individual patients and differentiated into specific cell types. To develop new therapies, the resultant cells are used to observe disease-specific phenotypes and identify novel pathological mechanisms,. Human iPSC-based disease modeling with patient-specific cells now provides an exciting new approach for the development of personalized diagnosis and medicine.

Figure 2

A schematic for human iPSCs-based

Figure 2

A schematic for human iPSCs-based cell therapy. Human iPSC-based cell therapy development usually

A schematic for human iPSCs-based cell therapy. Human iPSC-based cell therapy development usually includes the following steps: 1) Collect somatic cells from patients and culture somatic cells from affected patients; 2) Reprogram patient somatic cells into iPSCs; 3) Use genome editing technology or viral transduction method to repair patient iPSCs and turn them into genetically corrected iPSCs; 4) Differentiate the corrected iPSCs into desired cell types to serve as genetically matched healthy donor cells; 5) Perform quality control test for cell identity, purity, activity, and safety; and 6) Transplant the genetically matched healthy cells into patients for cell therapy.

Doss MX, Sachinidis A. Doss MX, et al. Cells. 2019 Apr 30;8(5):403. doi: 10.3390/cells8050403. Cells. 2019. PMID: 31052294 Free PMC article. Review.

Wang F, Kong J, Cui YY, Liu P, Wen JY. Wang F, et al. Chin Med J (Engl). 2018 Apr 5;131(7):852-856. doi: 10.4103/0366-6999.228231. Chin Med J (Engl). 2018. PMID: 29578130 Free PMC article. Review.

Wattanapanitch M. Wattanapanitch M. Stem Cells Int. 2019 May 2;2019:5171032. doi: 10.1155/2019/5171032. eCollection 2019. Stem Cells Int. 2019. PMID: 31191673 Free PMC article. Review.

Nsair A, MacLellan WR. Nsair A, et al. Adv Drug Deliv Rev. 2011 Apr 30;63(4-5):324-30. doi: 10.1016/j.addr.2011.01.013. Epub 2011 Mar 1. Adv Drug Deliv Rev. 2011. PMID: 21371511 Free PMC article. Review.

Cai CY, Meng FL, Rao L, Liu YY, Zhao XL. Cai CY, et al. Yi Chuan. 2020 Nov 20;42(11):1042-1061. doi: 10.16288/j.yczz.20-235. Yi Chuan. 2020. PMID: 33229312 Review. Chinese.

Pilipovi K, Harej Hrka A, Kui N, Mri-Peli J. Pilipovi K, et al. Biomedicines. 2022 Dec 29;11(1):94. doi: 10.3390/biomedicines11010094. Biomedicines. 2022. PMID: 36672601 Free PMC article. Review.

Lien CY, Chen TT, Tsai ET, Hsiao YJ, Lee N, Gao CE, Yang YP, Chen SJ, Yarmishyn AA, Hwang DK, Chou SJ, Chu WC, Chiou SH, Chien Y. Lien CY, et al. Cells. 2023 Jan 4;12(2):211. doi: 10.3390/cells12020211. Cells. 2023. PMID: 36672144 Free PMC article.

Akbarzadeh A, Sobhani S, Soltani Khaboushan A, Kajbafzadeh AM. Akbarzadeh A, et al. Bioengineering (Basel). 2023 Jan 12;10(1):106. doi: 10.3390/bioengineering10010106. Bioengineering (Basel). 2023. PMID: 36671678 Free PMC article. Review.

Han JL, Entcheva E. Han JL, et al. Stem Cell Rev Rep. 2023 Jan 19:1-20. doi: 10.1007/s12015-023-10506-4. Online ahead of print. Stem Cell Rev Rep. 2023. PMID: 36656467 Free PMC article. Review.

Mohd Satar A, Othman FA, Tan SC. Mohd Satar A, et al. World J Stem Cells. 2022 Dec 26;14(12):851-867. doi: 10.4252/wjsc.v14.i12.851. World J Stem Cells. 2022. PMID: 36619694 Free PMC article.

Cite

Format: AMA APA MLA NLM

Read more:
Induced pluripotent stem cell technology: a decade of progress

Induced Pluripotent Stem Cells (iPSCs)-Roles in Regenerative Therapies …

Title & authors Abstract Conflict of interest statement Figures Similar articles Cited by References Publication types MeSH terms Related information Grant support LinkOut - more resources

Review

Affiliations Expand

Item in Clipboard

Review

Mourad A M Aboul-Soudet al. Cells. 2021.

Display options

Format Abstract PubMed PMID

Item in Clipboard

Display options

Format Abstract PubMed PMID

The discovery of induced pluripotent stem cells (iPSCs) has made an invaluable contribution to the field of regenerative medicine, paving way for identifying the true potential of human embryonic stem cells (ESCs). Since the controversy around ethicality of ESCs continue to be debated, iPSCs have been used to circumvent the process around destruction of the human embryo. The use of iPSCs have transformed biological research, wherein increasing number of studies are documenting nuclear reprogramming strategies to make them beneficial models for drug screening as well as disease modelling. The flexibility around the use of iPSCs include compatibility to non-invasive harvesting, and ability to source from patients with rare diseases. iPSCs have been widely used in cardiac disease modelling, studying inherited arrhythmias, neural disorders including Alzheimer's disease, liver disease, and spinal cord injury. Extensive research around identifying factors that are involved in maintaining the identity of ESCs during induction of pluripotency in somatic cells is undertaken. The focus of the current review is to detail all the clinical translation research around iPSCs and the strength of its ever-growing potential in the clinical space.

Keywords: disease; drug screening; embryo; induced pluripotent stem cells; modelling.

The authors declare that they have no conflict of interest.

Figure 1

Showing the process of progression

Figure 1

Showing the process of progression and generating iPSC cells. Detailed description of creating

Showing the process of progression and generating iPSC cells. Detailed description of creating iPSCs with reprogramming factors and differentiating them into a variety of cell types.

Figure 2

Schematic representation on derivation and

Figure 2

Schematic representation on derivation and assay for human iPSCs. Detailed schematic representation of

Schematic representation on derivation and assay for human iPSCs. Detailed schematic representation of derivation of iPSC with the various assays to evaluate the developmental efficiency.

Figure 3

Process of liver development and

Figure 3

Process of liver development and hepatic differentiation from hiPSCs. The process of isolated

Process of liver development and hepatic differentiation from hiPSCs. The process of isolated cells from patients can be cultured and reprogrammed into patient-specific hiPSCs and quick comparison from natural liver development.

Skalova S, Svadlakova T, Shaikh Qureshi WM, Dev K, Mokry J. Skalova S, et al. Int J Mol Sci. 2015 Feb 13;16(2):4043-67. doi: 10.3390/ijms16024043. Int J Mol Sci. 2015. PMID: 25689424 Free PMC article. Review.

Ohnuki M, Takahashi K. Ohnuki M, et al. Philos Trans R Soc Lond B Biol Sci. 2015 Oct 19;370(1680):20140367. doi: 10.1098/rstb.2014.0367. Philos Trans R Soc Lond B Biol Sci. 2015. PMID: 26416678 Free PMC article. Review.

Valdimarsdttir G, Richter A. Valdimarsdttir G, et al. Laeknabladid. 2015 Dec;101(12):581-6. doi: 10.17992/lbl.2015.12.56. Laeknabladid. 2015. PMID: 26656400 Review. Icelandic.

Parrotta EI, Scalise S, Scaramuzzino L, Cuda G. Parrotta EI, et al. Int J Mol Sci. 2019 Nov 16;20(22):5760. doi: 10.3390/ijms20225760. Int J Mol Sci. 2019. PMID: 31744081 Free PMC article. Review.

Okano H, Nakamura M, Yoshida K, Okada Y, Tsuji O, Nori S, Ikeda E, Yamanaka S, Miura K. Okano H, et al. Circ Res. 2013 Feb 1;112(3):523-33. doi: 10.1161/CIRCRESAHA.111.256149. Circ Res. 2013. PMID: 23371901 Review.

Ng WC, Lokanathan Y, Baki MM, Fauzi MB, Zainuddin AA, Azman M. Ng WC, et al. Biomedicines. 2022 Nov 30;10(12):3082. doi: 10.3390/biomedicines10123082. Biomedicines. 2022. PMID: 36551838 Free PMC article. Review.

Shakir S, Hackett TL, Mostao-Guidolin LB. Shakir S, et al. Front Bioeng Biotechnol. 2022 Oct 28;10:1011800. doi: 10.3389/fbioe.2022.1011800. eCollection 2022. Front Bioeng Biotechnol. 2022. PMID: 36394026 Free PMC article. Review.

Alberti G, Russo E, Corrao S, Anzalone R, Kruzliak P, Miceli V, Conaldi PG, Di Gaudio F, La Rocca G. Alberti G, et al. Biomedicines. 2022 Nov 5;10(11):2822. doi: 10.3390/biomedicines10112822. Biomedicines. 2022. PMID: 36359342 Free PMC article. Review.

Linkova DD, Rubtsova YP, Egorikhina MN. Linkova DD, et al. Cells. 2022 Aug 29;11(17):2691. doi: 10.3390/cells11172691. Cells. 2022. PMID: 36078098 Free PMC article. Review.

Li XW, Lu YY, Zhang SY, Sai NN, Fan YY, Cheng Y, Liu QS. Li XW, et al. Front Pharmacol. 2022 Jun 22;13:926123. doi: 10.3389/fphar.2022.926123. eCollection 2022. Front Pharmacol. 2022. PMID: 35814256 Free PMC article.

Show all 116 references

Cite

Format: AMA APA MLA NLM

Read more:
Induced Pluripotent Stem Cells (iPSCs)-Roles in Regenerative Therapies ...