Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Tamibarotene + arsenic trioxide is a combination therapy investigated for the treatment of relapsed or refractory acute promyelocytic leukemia (APL). Tamibarotene (Am80) is a synthetic retinoid and a selective agonist of the retinoic acid receptors alpha (RARα) and beta (RARβ), designed to induce terminal differentiation of leukemic cells and overcome resistance to all-trans retinoic acid (ATRA). Arsenic trioxide (ATO) is an antineoplastic agent that induces apoptosis and promotes the degradation of the PML-RARα fusion protein. This combination was evaluated in a Phase I clinical trial led by Northwestern University's Robert H. Lurie Comprehensive Cancer Center, with tamibarotene provided by CytRx Corporation, to determine the safety and efficacy of the regimen in patients who had relapsed after standard frontline therapy.
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 tamibarotene + arsenic trioxide.