Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
EIS-12656 is a first-in-class, orally bioavailable small molecule that acts as an allosteric inhibitor of the chromatin helicase ALC1 (also known as CHD1L). Developed by Eisbach Bio, this agent selectively targets and inhibits ALC1 activity in tumor cells, thereby preventing ALC1/poly(ADP-ribose) polymerase (PARP)-mediated repair of DNA breaks. By suppressing cancer-relevant genome reorganization induced by DNA damage, EIS-12656 leads to chromatin trapping and cancer cell death. The drug is designed for the treatment of advanced solid tumors—particularly those deficient in homologous recombination repair pathways or resistant to PARP inhibitors. Preclinical studies have demonstrated substantial tumor growth inhibition, blood-brain barrier penetration, and a favorable safety profile. Clinical development is ongoing with phase 1/2 trials evaluating its use both as monotherapy and in combination with standard-of-care therapies[2][5][7][9].
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 EIS-12656.