Vedanta Biosciences starts phase 1 study of VE202 to treat IBD
US-based Vedanta Biosciences has started a phase I clinical study of its live biotherapeutic product (LBP) candidate VE202 to treat inflammatory bowel disease (IBD).
US-based Vedanta Biosciences has started a phase I clinical study of its live biotherapeutic product (LBP) candidate VE202 to treat inflammatory bowel disease (IBD).
Contract research organization (CRO) QPS has expanded its US-based phase I clinical trial capabilities to support the increasing requirements of its pharmaceutical, biotechnology and CRO partners.
Bristol-Myers Squibb (BMS) announced that its cancer drug combination Opdivo plus Yervoy has failed to improve overall survival (OS) rate in the phase 3 CheckMate -451 study.
Biopharmaceutical company Poxel has stared part 2 of the phase 1a study for PXL065, a deuterium-stabilized R-stereoisomer of pioglitazone.
Actinogen Medical has enrolled the final patient into XanADu, a phase 2 clinical trial to evaluate Xanamem in the treatment of patients with mild Alzheimer’s disease.
Pfizer and Merck have announced that avelumab alone or in combination with pegylated liposomal doxorubicin (PLD) has failed to improve overall survival (OS) or progression-free survival (PFS) rate in phase III Javelin Ovarian 200 trial.
GlycoMimetics has dosed the first patient in its Phase 3 clinical trial of uproleselan (GMI-1271) in relapsed/refractory acute myeloid leukemia (AML).
AstraZeneca’s Imfinzi (durvalumab) monotherapy and the combination of Imfinzi with remelimumab have failed to improve overall survival (OS) rate in phase III Mystic lung cancer trial.
Seattle Genetics has dosed the d first patient in a phase 1 clinical trial evaluating the safety and tolerability of SEA-BCMA for patients with relapsed or refractory multiple myeloma (MM).
Merck has announced that its anti-PD-1 therapy Keytruda (pembrolizumab) significantly improved overall survival (OS) rate in the phase 3 Keynote-181 esophageal cancer trial.