Recent blog posts
OKYO Pharma Corp. reports that OK-101 hit key efficacy goals in its Phase 2 trials, effectively treating dry eye syndrome
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OKYO Pharma Corp. reports that OK-101 hit key efficacy goals in its Phase 2 trials, effectively treating dry eye syndrome
13 January 2024
OKYO Pharma Corporation has disclosed that OK-101 has met its primary efficacy benchmarks in Phase 2 human trials, demonstrating statistical relevance in treating dry eye condition.
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Scemblix® by Novartis shows superior efficacy in a Phase III trial, significantly increasing molecular remission rates for new chronic myeloid leukemia cases
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Scemblix® by Novartis shows superior efficacy in a Phase III trial, significantly increasing molecular remission rates for new chronic myeloid leukemia cases
13 January 2024
Novartis' Scemblix® outperforms traditional therapy in achieving significant molecular remission in a Phase III study involving newly diagnosed chronic myeloid leukemia patients.
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Caliway Announces FDA Phase II Trial Approval for Dercum's Syndrome Candidate CBL-514
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Caliway Announces FDA Phase II Trial Approval for Dercum's Syndrome Candidate CBL-514
13 January 2024
Caliway Reveals US FDA Approval for Phase II Trial Application of CBL-514, a Sham-Controlled Study Aiming to Address Dercum's Syndrome.
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UCB announces EU approval for RYSTIGGO as an adult generalized myasthenia gravis treatment
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UCB announces EU approval for RYSTIGGO as an adult generalized myasthenia gravis treatment
13 January 2024
UCB has revealed that the European Commission has sanctioned the use of RYSTIGGO (rozanolixizumab) for treating generalized myasthenia gravis in adult patients across Europe.
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OBI Pharma announced FDA approval for a Phase 1/2 trial of its TROP2 ADC, OBI-992
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OBI Pharma announced FDA approval for a Phase 1/2 trial of its TROP2 ADC, OBI-992
13 January 2024
OBI Pharma has disclosed that the FDA has given its approval for a Phase 1/2 clinical trial application concerning OBI-992, a TROP2 antibody-drug conjugate.
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AskBio Commences Phase 2 Clinical Study of GenePHIT in Heart Failure Treatment
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AskBio Commences Phase 2 Clinical Study of GenePHIT in Heart Failure Treatment
13 January 2024
Asklepios BioPharmaceutical, Inc., a wholly-owned subsidiary of Bayer AG, has launched Phase II of the GenePHIT trial to assess the effectiveness of its gene therapy drug AB-1002 (NAN-101) for congestive heart failure.
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Sana Biotech's SC262, a CD22-targeted CAR T cell therapy for resistant B-cell cancers, gains US regulatory approval
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Sana Biotech's SC262, a CD22-targeted CAR T cell therapy for resistant B-cell cancers, gains US regulatory approval
13 January 2024
Sana Biotech Reveals US Regulatory Approval for Experimental Drug SC262, an Engineered Immune-resistant, Targeted CD22 Allo CAR T Cell Treatment, Aimed at Individuals Suffering from Recurring or Resistant Types of B-cell Cancer.
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Boston Pharma Debuts BOS-580 Study at 2024 NASH-TAG, Highlights Lasting Low Immune Response for MASH Treatment
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Boston Pharma Debuts BOS-580 Study at 2024 NASH-TAG, Highlights Lasting Low Immune Response for MASH Treatment
10 January 2024
Boston Pharmaceuticals Unveils Research at the 2024 NASH-TAG Showing Sustained Low Immune Reaction to their Extended-release FGF21 Mimic, BOS-580, in MASH Management.
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Ligand Pharmaceuticals Inc. announces ZELSUVMI™ FDA approval for treating molluscum contagiosum in adults and children over 1 year old
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Ligand Pharmaceuticals Inc. announces ZELSUVMI™ FDA approval for treating molluscum contagiosum in adults and children over 1 year old
10 January 2024
Ligand Pharmaceuticals Inc. has announced FDA approval for ZELSUVMI™ (berdazimer topical gel, 10.3%), now approved to treat molluscum contagiosum in adults and children aged 1 and older.
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BioPharma Accord, Inc. announces FDA approval for their STELARA® biosimilar, DMB-3115 license application
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BioPharma Accord, Inc. announces FDA approval for their STELARA® biosimilar, DMB-3115 license application
10 January 2024
BioPharma Accord, Inc. reports the U.S. FDA has greenlit their application for a license regarding their proposed biosimilar to STELARA®, named DMB-3115.
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Innate Pharma's Lacutamab Clinical Program resumes with FDA's approval after lifting previous partial hold
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Innate Pharma's Lacutamab Clinical Program resumes with FDA's approval after lifting previous partial hold
10 January 2024
Innate Pharma has been given the green light by the FDA to resume its Lacutamab Clinical Program after the previous partial clinical hold was removed.
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Avenzo Therapeutics unveils promising CDK2 inhibitor AVZO-021, originally from Allorion Therapeutics
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Avenzo Therapeutics unveils promising CDK2 inhibitor AVZO-021, originally from Allorion Therapeutics
10 January 2024
Avenzo Therapeutics has disclosed the promising clinical phase CDK2 inhibitor known as AVZO-021, originally developed by Allorion Therapeutics.
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