Recruiting nowPhase 1Ages 16 Years and up
A Phase 1/1B Study of ST-01156, a Small Molecule RBM39 Degrader, in Patients With Advanced Solid Malignancies
Sponsor: SEED Therapeutics, Inc. · NCT07197554 on ClinicalTrials.gov ↗
Conditions studied
Advanced Solid TumorsEwing SarcomaHepatocellular Carcinoma (HCC)Biliary Tract Cancer (BTC)
What it tests
- ST-01156drug
Where it's running6 sites
- Recruiting now
The City of Hope National Medical Center
Duarte, California 91010
- Kathryn Zurcher(contact)626-218-3029[email protected]
- Daneng Li(principal investigator)
- Recruiting now
Hoag Memorial Hospital
Newport Beach, California 92263
- Holland Orndorff(contact)949-764-7110[email protected]
- Alain Mita(principal investigator)
- Recruiting now
Mass General Brigham Cancer Institute
Boston, Massachusetts 02114
- Kristina Goodwin(contact)617-643-6256[email protected]
- Gregory Cote(principal investigator)
- Recruiting now
Dana Farber Cancer Institute
Boston, Massachusetts 02215
- Suzanne George(contact)877-338-7425[email protected]
- Suzanne George, MD(principal investigator)
- Recruiting now
Memorial Sloan Kettering Cancer Center
New York, New York 10065
- Pri Wartanian(contact)210-685-2159[email protected]
- Robert Maki(principal investigator)
- Recruiting now
The University of Texas MD Anderson Cancer Center
Houston, Texas 77030
- Kofi Effa Ababio(contact)346-725-3989[email protected]
- Jordi Rodon Ahnert(principal investigator)
See the official eligibility language
Shown exactly as written on ClinicalTrials.gov. Your oncologist is the right person to judge whether it fits your situation.
Inclusion Criteria: * Age ≥ 18 years on the day of signing the consent form, except for adolescents with Ewing Sarcoma or other malignancies for which there is a biological rationale to support participation, in which case the participant is ≥ 16 years old. * Has a metastatic or locally advanced and unresectable solid tumor. * Has at least 1 measurable lesion or evaluable disease per RECIST v1.1. * Has an ECOG performance status ≤ 2 at screening. * Has adequate organ function as defined in the protocol. Exclusion Criteria: * Has received prior radiotherapy within 2 weeks of treatment. * Has known active CNS metastases and/or carcinomatous meningitis. Participants with previously treated brain metastases may participate, provided they are radiologically stable * Has received treatment with any local or systemic anticancer therapy or investigational anticancer agent within 14 days or 5 half-lives, whichever is shorter. * Had major surgery within 28 days before study therapy administration * Has toxicities from previous anticancer therapies that have not resolved to baseline levels, with the exception of alopecia and peripheral neuropathy. * Has previously received a RBM39 inhibitor/degrader.
Updated 2026-06-02 on ClinicalTrials.gov. Always confirm current details with the study team or your oncologist.