Recruiting nowPhase 1/2Ages 18 Years and up
STC-15 as a Part of Combination Therapy With Toripalimab in Selected Advanced Cancers and as Monotherapy in Participants With Selected Sarcomas
Sponsor: STORM Therapeutics LTD · NCT06975293 on ClinicalTrials.gov ↗
Conditions studied
Solid TumorSarcomaLeiomyosarcomaDedifferentiated Liposarcoma
What it tests
- STC-15 in combination with toripalimabcombination_product
- STC-15 monotherapydrug
Where it's running6 sites
- Recruiting now
Northwell Health Cancer Institute
Lake Success, New York 11042
- Serena Petruzzelli(contact)[email protected]
- Anthony Philip, MD(principal investigator)
- Recruiting now
NEXT Houston
Houston, Texas 77054
- Emma Morales(contact)832-384-7912[email protected]
- Jennifer Segar, MD(principal investigator)
- Recruiting now
NEXT Dallas
Irving, Texas 75039
- Mofopefoluwa Akinwale(contact)972-893-8800[email protected]
- Faran Polani, MD(principal investigator)
- Recruiting now
NEXT Oncology
San Antonio, Texas 78229
- Jordan Georg(contact)210-580-9521[email protected]
- Ildefonso I Rodriguez Rivera, MD(principal investigator)
- Recruiting now
The START Center
San Antonio, Texas 78229
- Isabel Jimenez, RN, MSN(contact)210-593-5265[email protected]
- Kyriakos Papadopoulos, MD(principal investigator)
- Recruiting now
NEXT Oncology
Fairfax, Virginia 22031
- Blake Patterson(contact)703-783-4505[email protected]
- M. Adham Salkeni, MD, FRCPC(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.
Key Inclusion Criteria: * Estimated life expectancy ≥ 3 months. * ECOG performance status 0 or 1. * Measurable disease according to RECIST v1.1 as assessed by the local site investigator/radiology. * Documented radiologic assessment of progression on the prior therapy before study entry. * Have adequate organ function. * Have the ability to swallow, retain, and absorb oral medication. Inclusion Criteria (Phase 2 Monotherapy Cohorts): * Have histologic or cytologic confirmation of advanced sarcoma of the selected histologic subtype that is not amenable to local curative therapy. Participant must have received at least 2, but no more than 4 prior lines of systemic therapy. * Pre-treatment and on-treatment biopsy if medically feasible. Key Exclusion Criteria: * Pregnant and lactating women. * Received prior systemic anticancer therapy including investigational agents within 4 weeks or 5 half-lives, whichever is shorter, prior to first IMP administration. * Participants who have not recovered from all AEs due to previous therapies to Grade ≤ 1 or baseline, according to NCI-CTCAE v5.0. Exceptions include: alopecia, Grade ≤ 2 neuropathy, and endocrine-related AEs Grade ≤ 2 who are stable on treatment or hormone replacement. * History of (non-infectious) pneumonitis/interstitial lung disease that required steroids or the presence of ongoing pneumonitis/interstitial lung disease). * Clinically significant cardiovascular disease or condition. * Known active CNS metastases and/or leptomeningeal disease.
Updated 2026-04-21 on ClinicalTrials.gov. Always confirm current details with the study team or your oncologist.