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Terns Pharmaceuticals Highlights New Preclinical Data Supporting TERN-501 in Combination with a GLP-1R Agonist for Obesity at the ADA’s 84th Annual…

TERN-501 significantly improved the efficacy of a GLP-1 receptor agonist by normalizing energy expenditure, resulting in greater weight loss, increased fat mass loss and relative preservation of lean mass TERN-501 significantly improved the efficacy of a GLP-1 receptor agonist by normalizing energy expenditure, resulting in greater weight loss, increased fat mass loss and relative preservation of lean mass

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Terns Pharmaceuticals Highlights New Preclinical Data Supporting TERN-501 in Combination with a GLP-1R Agonist for Obesity at the ADA’s 84th Annual...

Roche launches new analytical units for cobas® pro integrated solutions delivering greater efficiency and capacity to laboratories

Basel, 24 June 2024 - Roche (SIX: RO, ROG; OTCQX: RHHBY) announced today the launch of its new analytical units, cobas® c 703 and cobas® ISE neo, for the cobas® pro integrated solutions, in countries accepting the CE mark. The cobas pro integrated solutions is a scalable and modular diagnostic platform designed for high-volume laboratories. The cobas c 703 and cobas ISE neo analytical units offer cutting-edge features to help address some of the key challenges faced by diagnostic laboratories worldwide such as shortage of qualified staff and space limitations.

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Roche launches new analytical units for cobas® pro integrated solutions delivering greater efficiency and capacity to laboratories

AstriVax enters clinical phase with its novel vaccine platform technology

Leuven - June 24, 2024 - The first participants have been dosed in a Phase I clinical study to test the safety and efficacy of AstriVax’s prophylactic vaccines for yellow fever (AVX70120) and rabies (AVX70481) in healthy adults. The first-in-human safety and immunogenicity data generated by this study will be a stepping stone in advancing AstriVax immunotherapies to clear chronic infections such as Hepatitis B and human papillomavirus (HPV) infections.

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AstriVax enters clinical phase with its novel vaccine platform technology

Altimmune Presents Data from Phase 2 MOMENTUM Trial of Pemvidutide in Obesity during Oral Presentation at the American Diabetes Association’s 84th…

Full analysis of body composition data showed class-leading lean mass preservation with 21.9% of weight loss attributable to lean mass and 78.1% attributable to fat Full analysis of body composition data showed class-leading lean mass preservation with 21.9% of weight loss attributable to lean mass and 78.1% attributable to fat

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Altimmune Presents Data from Phase 2 MOMENTUM Trial of Pemvidutide in Obesity during Oral Presentation at the American Diabetes Association’s 84th...

Novo Nordisk A/S: Mim8 demonstrated superior reductions in annualised bleeding rate (ABR) compared to on-demand and prior prophylaxis treatment in…

FRONTIER2 data presented at ISTH 2024 showed that up to 95% of people, who had no prior prophylaxis treatment, experienced zero treated bleeds while on Mim8

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Novo Nordisk A/S: Mim8 demonstrated superior reductions in annualised bleeding rate (ABR) compared to on-demand and prior prophylaxis treatment in...

Valneva Announces Health Canada Approval of the World’s First Chikungunya Vaccine, IXCHIQ®

Saint-Herblain (France), June 24, 2024 – Valneva SE (Nasdaq: VALN; Euronext Paris: VLA), a specialty vaccine company, today announced that Health Canada has approved IXCHIQ®, Valneva’s single-dose vaccine for the prevention of disease caused by the chikungunya virus in individuals 18 years of age and older. This decision marks the second approval the Company has received for IXCHIQ® following approval from the U.S. Food and Drug Administration (FDA) in November 2023. The European Medicines Agency (EMA) also recently recommended marketing authorization of the vaccine in Europe, and a formal decision is expected in the third quarter of 2024.

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Valneva Announces Health Canada Approval of the World’s First Chikungunya Vaccine, IXCHIQ®

Stem Cell Therapy Market to Triple, Reaching USD 52.1 Billion by 2034 at a 12.1% of CAGR – PharmiWeb.com

Stem Cell Therapy Market

The stem cell therapy market is on the brink of explosive growth, with a compound annual growth rate (CAGR) of 12.1% projected over the next decade. Starting at an estimated value of USD 16.7 billion in 2024, the market is expected to surge to an impressive USD 52.1 billion by 2034.

This significant expansion reflects the increasing adoption of stem cell therapies, driven by their potential to revolutionize treatment for a wide range of conditions. From regenerative medicine to chronic disease management, stem cell therapy is unlocking new possibilities in medical science.

As research continues to advance and clinical applications expand, the stem cell therapy market is set to play a pivotal role in transforming healthcare and improving patient outcomes worldwide. This remarkable growth trajectory underscores the importance of continued investment and innovation in this cutting-edge field.

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Competitive Landscape

The market is very competitive because there are many top biotech and pharmaceutical companies in it. It is distinguished by fierce rivalry, quick technical progress, and a significant amount of R&D activity focused on creating cutting-edge stem cell treatments. Businesses are making significant investments in R&D projects with the goal of creating innovative stem cell treatments for a variety of illnesses.

Recent Development in the Stem Cell Therapy Market

A strategic partnership was established in 2020 between Cipla and Stempeutics to launch Stempucel, a revolutionary stem cell therapy for the management of critical limb ischemia. The partnership aims to increase their market share in this quickly developing industry and capitalize on the rising demand for stem cell therapy. Millions of individuals worldwide suffer from critical limb ischemia, a crippling illness for which the introduction of Stempucel is predicted to change the course of therapy.

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Stem Cell Therapy Market to Triple, Reaching USD 52.1 Billion by 2034 at a 12.1% of CAGR - PharmiWeb.com