Tag: clinical trial

Cabaletta Bio’s IND application for CABA-201 to treat systemic lupus erythematosus has been approved by the US FDA.

The US Food and Drug Administration has approved the company’s investigational new drug (IND) application for CABA-201, a fully human CD19-CAR T cell investigational therapy that contains the 4-1BB protein, according to Cabaletta Bio, Inc., a clinical-stage biotechnology company focused…

Apply for the post of Clinical Research Associates and Clinical Trial Assistant at Teva Pharmaceuticals – B. Pharma/ M. Pharma/ M. Sc.

Clinical Research department in Teva supports Protocols, Bioanalysis, CDISC, Final Reports, eTMF, Data Management. It also provides bioanalysis to support Teva studies in various other countries. Teva India Clinical Research team does monitoring to support Teva Israel/ Europe & US…

Apply for Medical Service Associate (Pharmacovigilance) at Accenture – B. Pharma/ M. Pharma

Global professional services provider Accenture has industry-leading expertise in digital, cloud, and security. We provide Strategy and Consulting, Technology and Operations services, and Accenture Song, all powered by the greatest global network of Advanced Technology and Intelligent Operations centres, combining…

Positive findings from the second interim analysis of the phase 2 randomised trial for BX1000 are reported by Baudax Bio.

The second preplanned interim analysis of Baudax Bio, Inc.’s phase 2 trial of BX1000 for neuromuscular blockade (NMB) in patients undergoing elective surgery showed promising results. Baudax Bio, Inc. is a pharmaceutical company that specialises in developing novel products for…

The US FDA designates Intellia’s NTLA-2002, a regenerative medicine advanced therapy to treat hereditary angioedema.

The US Food and Drug Administration (FDA) has designated NTLA-2002 for the treatment of hereditary angioedema as a Regenerative Medicine Advanced Treatment (RMAT), according to Intellia Therapeutics, Inc., a leading clinical-stage genome editing business (HAE). NTLA-2002 is a CRISPR-based in…

Phase 1 patient dosing of PT886 for advanced gastric, gastroesophageal junction, and pancreatic adenocarcinomas is initiated by Phanes Therapeutics.

First patient dosed in phase 1 clinical study (NCT05482893) of PT886, a first-in-class native IgG-like bispecific antibody (bsAb) targeting claudin 18.2 and CD47 for the treatment of gastric, gastroesophageal junction, and pancreatic adenocarcinomas, according to Phanes Therapeutics, Inc. (Phanes), an…

Back to top

Registration Form


This will close in 0 seconds

This will close in 0 seconds

WhatsApp Join Telegram