Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Remtolumab (ABT-122) is a novel dual-variable domain immunoglobulin (DVD-Ig™) engineered to simultaneously and selectively neutralize both tumor necrosis factor alpha (TNFα) and interleukin-17A (IL-17A). It was developed as a bispecific monoclonal antibody for the treatment of autoimmune diseases such as rheumatoid arthritis and psoriatic arthritis. The drug was designed to combine the therapeutic effects of TNF inhibition with IL-17A blockade in a single molecule, aiming to improve efficacy over existing monotherapies. Clinical trials demonstrated that ABT-122 had similar safety and efficacy profiles compared to adalimumab but did not show clear superiority; development has since been discontinued for its primary indications[1][2][3][4][5].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on remtolumab.