An IND application is a request for authorization from the FDA ... of detail needed for the IRB and/or FDA to make a determination. Learn more on the FDA process Here is where differences become our ...

Tuesday announced its plan to file an Investigational New Drug or IND application with the U.S. FDA in 2025 to support a first-in-human clinical study of its small-diameter acellular tissue ...

From the time an IND application is submitted to the FDA until the IND ... and when Tracking through a change control process all amendments to FDA-cleared IND applications, such as new protocols or ...

Tiziana Life Sciences (NASDAQ:TLSA) rises after the company said it is planning the submission of its Investigational New ...

has cleared the company’s Investigational New Drug (IND) application for LTZ-301, a first-in-class myeloid engager immunotherapy intended to treat relapsed or refractory non-Hodgkin lymphoma (r ...