An arbitration panel ruled Prime did not violate an agreement with Beam when it developed PM647, for which Prime plans to launch a clinical trial.
Current Chemolab equity holders will own approximately 32 percent of the combined company' shares and Scipher equity holders will own 68 percent.
The RNA silencer Wainua didn't improve outcomes for ATTR-CM patients who were already receiving the standard of care.
The firm will use the proceeds to develop plixorafenib in BRAF-mutant brain tumors and possibly make a regulatory submission.
The deal involves non-dilutive cash in exchange for royalties, if the gene therapies are approved, and an equity investment from Oberland Capital.
The biotech is tackling common cardiovascular conditions by targeting risk factors like high cholesterol, triglycerides, and ...
The firm announced it has aligned with the US Food and Drug Administration on the design of the Phase III study, which could support a biologics license application.
The partnership will leverage Sanyou's AI-based libraries of over one trillion antibody gene sequences and Baiyunshan Xihe's supply chain expertise.
NEW YORK – The US Food and Drug Administration has accepted two supplemental new drug applications (sNDAs) seeking to convert accelerated approvals for two of Sarepta Therapeutics' Duchenne muscular ...
Houston biopharma company CoRegen said it has received US Food and Drug Administration clearance to begin a Phase I/II trial of CRG-150, an adoptive cell therapy targeting steroid receptor coactivator ...
Spur Therapeutics on Tuesday said it has treated the first Gaucher disease patient with its investigational gene therapy, FLT201 (avigbagene parvec), in a pivotal trial. In the Phase III GALILEO-3 ...
The gene therapy for multiple sulfatase deficiency was one of the preclinical programs the Bespoke Gene Therapy Consortium selected for its pilot.
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