Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at San Francisco, California and other locations
Dates
study started
study ends around
Principal Investigator
by Varun Monga, MBBS
Headshot of Varun Monga
Varun Monga

Description

Summary

This early phase oncology trial will be conducted at various study centers to investigate the safety, tolerability, and antitumor activity of STC-15 (a METTL3 inhibitor) in combination with toripalimab (anti- programmed cell death 1 [PD-1]) in advanced unresectable or metastatic tumors.

The Phase 2 Monotherapy part is an open-label, non-randomized, multicenter Simon's 2-stage design that investigates the safety, tolerability, and antitumor activity of STC-15 in participants with selected, relapsed sarcomas subtypes, dedifferentiated (DD) liposarcoma and leiomyosarcoma (uterine and non-uterine).

Official Title

Open-label, Non-randomized, Multi-cohort, Phase 1b/2 Trial Investigating the Safety, Tolerability, and Antitumor Activity of STC-15 (a METTL3 Inhibitor) as a Part of Combination Therapy With Toripalimab in Participants With Selected Advanced Cancers and as Monotherapy in Participants With Selected Sarcomas

Keywords

Solid Tumor, Sarcoma, Leiomyosarcoma, Dedifferentiated Liposarcoma, STC-15, Toripalimab, PD1, Checkpoint Combination, Liposarcoma, STC-15 in combination with toripalimab, STC-15 monotherapy

Eligibility

You can join if…

Open to people ages 18 years and up

  • 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.

You CAN'T join if...

  • 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.

Locations

  • UCSF accepting new patients
    San Francisco California 94158 United States
  • NEXT Dallas accepting new patients
    Irving Texas 75039 United States
  • NEXT Oncology accepting new patients
    San Antonio Texas 78229 United States
  • The START Center accepting new patients
    San Antonio Texas 78229 United States

Lead Scientist at UCSF

  • Varun Monga, MBBS
    Dr. Varun Monga is a Board Certified Medical Oncologist who serves as an Clinical Associate Professor of Medicine in the Division of Hematology and Oncology. He joined UCSF Medical Center in 2023 and he provides patient care services limited to UCSF Sarcoma Center and Cancer Clinical Trials and Investigational Treatments Center.

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
STORM Therapeutics LTD
ID
NCT06975293
Phase
Phase 1/2 research study
Study Type
Interventional
Participants
Expecting 107 study participants
Last Updated