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Inactive Indication- |
Drug Highest PhasePhase 1 |
First Approval Ctry. / Loc.- |
First Approval Date- |
A Phase 1a/b Clinical Trial To Determine the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, Immunogenicity, and Efficacy of BB-TL1A-VIAL-HLE in Healthy Adult Volunteers and in Patients With Moderate-To-Severe Ulcerative Colitis
The goal of this clinical trial is to learn if BB-TL1A-VIAL-HLE is safe in healthy adults and is safe and effective in treating adults with moderate-to-severe ulcerative colitis. The main questions it aims to answer are:
Is the intervention safe in healthy adults and in adults with moderate-to-severe ulcerative colitis? Is the intervention effective in treating adults with moderate-to-severe ulcerative colitis? Researchers will compare the Phase 1b arm to a historical treatment arm to see if the study drug is at least as effective as a relevant benchmark.
Participants will:
* Attend the clinical research site several times over the course of
1 year
* Have blood and urine samples taken
* Undergo physical examinations
* Receive one injection of the study drug
100 Clinical Results associated with Battery Bio Australia Pty Ltd.
0 Patents (Medical) associated with Battery Bio Australia Pty Ltd.
100 Deals associated with Battery Bio Australia Pty Ltd.
100 Translational Medicine associated with Battery Bio Australia Pty Ltd.