Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06975293

STC-15 as a Part of Combination Therapy With Toripalimab in Selected Advanced Cancers and as Monotherapy in Participants With Selected Sarcomas

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).

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

University of California, San Francisco, San Francisco, California, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

STC-15 in combination with toripalimab

Combination Product

STC-15 in combination with toripalimab in 21-day cycles

STC-15 monotherapy

Drug

STC-15 monotherapy in 21-day cycles

Primary outcomes

  1. Combination Cohorts: Safety and tolerability of STC-15 in combination with toripalimab

    Time frame: 6 months

    Incidence of adverse events graded according to CTCAE v5.0

  2. Phase 2 Monotherapy Cohorts: Antitumor activity of STC-15 monotherapy

    Time frame: 6 months

    ORR according to RECIST

Secondary outcomes

  1. Combination Cohorts: Anti-tumor activity

    Time frame: 6 months

    To evaluate the antitumor activity of STC-15 in combination with toripalimab as per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 and immune RECIST (iRECIST) criteria

  2. Combination and Phase 2 Monotherapy Cohorts: Maximum observed plasma concentration of STC-15 (Cmax)

    Time frame: 22 days

  3. Combination and Phase 2 Monotherapy Cohorts: Calculated time to reach maximum observed plasma concentration (Tmax)

    Time frame: 22 days

  4. Combination and Phase 2 Monotherapy Cohorts: Calculated area under the plasma concentration-time curve of STC-15 (AUC0-t)

    Time frame: 22 days

  5. Phase 2 Monotherapy Cohorts: Safety and tolerability of STC-15

    Time frame: 6 months

    Incidence of adverse events graded according to CTCAE v5.0

Study contacts

Contact information is provided by the study sponsor or research team.

Melinda Snyder

CONTACT

[email protected]

617-233-4057

Sandra Tong, MD

CONTACT

[email protected]

650-399-6357

Sponsors and collaborators

Lead sponsor

STORM Therapeutics LTD

Industry

Collaborators

  • Coherus Oncology, Inc.

Registry information

Official study 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

Important dates

Study start
2025
Primary completion
2027
Study completion
2028
First posted
May 16, 2025
Registry last updated
Jul 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.