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| Name | Class |
|---|---|
| Coherus Oncology, Inc. | INDUSTRY |
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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).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Phase 1 dose escalation | Experimental | Phase 1b 3+3 trial design of dose escalation of STC-15 in combination with toripalimab |
|
| Phase 2 Stage 1 Monotherapy | Experimental | STC-15 in patients with DD liposarcoma or leiomyosarcoma |
|
| Phase 2 Stage 2 Monotherapy | Experimental | STC-15 in patients with DD liposarcoma or leiomyosarcoma |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| STC-15 in combination with toripalimab | Combination Product | STC-15 in combination with toripalimab in 21-day cycles |
|
| Measure | Description | Time Frame |
|---|---|---|
| Combination Cohorts: Safety and tolerability of STC-15 in combination with toripalimab | Incidence of adverse events graded according to CTCAE v5.0 | 6 months |
| Phase 2 Monotherapy Cohorts: Antitumor activity of STC-15 monotherapy | ORR according to RECIST | 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| Combination Cohorts: Anti-tumor activity | 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 | 6 months |
| Combination and Phase 2 Monotherapy Cohorts: Maximum observed plasma concentration of STC-15 (Cmax) |
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Key Inclusion Criteria:
Inclusion Criteria (Phase 2 Monotherapy Cohorts):
Key Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Sandra Tong, MD | Contact | 650-399-6357 | sandy.tong@stormtherapeutics.com | |
| Melinda Snyder | Contact | 617-233-4057 | melinda.snyder@stormtherapeutics.com |
| Name | Affiliation | Role |
|---|---|---|
| Sandra Tong, MD | Storm Therapeutics | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Northwell Health Cancer Institute | Recruiting | Lake Success | New York | 11042 | United States |
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| STC-15 monotherapy | Drug | STC-15 monotherapy in 21-day cycles |
|
| 22 days |
| Combination and Phase 2 Monotherapy Cohorts: Calculated time to reach maximum observed plasma concentration (Tmax) | 22 days |
| Combination and Phase 2 Monotherapy Cohorts: Calculated area under the plasma concentration-time curve of STC-15 (AUC0-t) | 22 days |
| Phase 2 Monotherapy Cohorts: Safety and tolerability of STC-15 | Incidence of adverse events graded according to CTCAE v5.0 | 6 months |
| NEXT Houston | Recruiting | Houston | Texas | 77054 | United States |
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| NEXT Dallas | Recruiting | Irving | Texas | 75039 | United States |
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| NEXT Oncology | Recruiting | San Antonio | Texas | 78229 | United States |
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| The START Center | Recruiting | San Antonio | Texas | 78229 | United States |
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| NEXT Oncology | Recruiting | Fairfax | Virginia | 22031 | United States |
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| ID | Term |
|---|---|
| D012509 | Sarcoma |
| D007890 | Leiomyosarcoma |
| D008080 | Liposarcoma |
| ID | Term |
|---|---|
| D018204 | Neoplasms, Connective and Soft Tissue |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D009379 | Neoplasms, Muscle Tissue |
| D018205 | Neoplasms, Adipose Tissue |
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| ID | Term |
|---|---|
| C000656314 | toripalimab |
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