Jacobio Pharma (1167.HK), a China-based pharmaceutical company, announced on Wednesday that it has submitted the Phase I/II Investigational New Drug (IND) application for its BET inhibitor JAB-8263 for the treatment of autoimmune diseases to the Centre for Drug Evaluation (CDE) in China and it has been accepted.
According to new regulatory guidelines, the review of JAB-8263's IND application is expected to be completed within 30 working days
Jacobio has previously completed phase I clinical trials of JAB-8263 for solid tumour and haematological malignancies in both China and the United States. Data presented at the 2024 American Society of Hematology (ASH) Annual Meeting showed that JAB-8263 demonstrated good tolerability.
The company says that JAB-8263 is an orally administered, highly potent BET inhibitor that it has developed independently. Its safety and pharmacokinetics have been evaluated in early phase trials in China and the United States. According to the company, JAB-8263 was well tolerated and exhibited a favourable PK profile. Jacobio is investigating the potential of JAB-8263 in solid tumours and autoimmune diseases.
Relay Therapeutics wins FDA breakthrough status for zovegalisib in breast cancer treatment
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Valneva and Instituto Butantan launch pilot chikungunya vaccination campaign in Brazil
Lupin launches Dasatinib tablets in US market
WuXi Biologics enters into licence and research service agreement with Vertex Pharmaceuticals
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
AstraZeneca agrees obesity and type 2 diabetes collaboration with CSPC
Ascletis Pharma Inc reports topline results from Phase III open-label study of denifanstat
Innovative Molecules GmbH completes Phase 1 clinical development programme for adibelivir
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA