A Study of the c-Kit Specific Antibody-Drug Conjugate NN3201 for Advanced and/or Metastatic Solid Tumors Known to Express c-Kit
Part of paid clinical trials in Ann Arbor, Michigan.
- Sponsor
- Novelty Nobility, Inc.
- Study ID
- NCT06805825
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Adenoid Cystic Carcinoma
- Chromophobe Renal Cell Carcinoma
- Clear Cell Renal Cell Carcinoma
- Gastrointestinal Stromal Tumors
- Neuroendocrine Tumors
- Small-cell Lung Cancer
- Uveal Melanoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- NN3201 — DRUGA c-Kit targeting fully human monoclonal antibody-drug conjugate with MMAE administered intravenously.
Study Details
This open-label clinical trial will evaluate the safety and tolerability of NN3201 in subjects with advanced and/or metastatic solid tumors known to express c-Kit.
Key Dates
- Start date
- Feb 3, 2025
- Status verified
- Sep 2025
- Primary completion
- Aug 30, 2027
- Completion
- Dec 31, 2027
Study Design
- Enrollment
- 67 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Part ANN3201 administered intravenously every three weeks, the dosage to be determined by ascending dose cohort assignment. Part A will enroll patients that have GIST or Other c-Kit tumor disease types. This is an open-label multiple ascending dose study.
- Experimental: Part B, Cohort 1 (GIST)NN3201 administered intravenously every three weeks, expanding one or two doses in GIST disease type. This is an open-label multiple dose expansion study.
- Experimental: Part B, Cohort 2 (SCLC)NN3201 administered intravenously every three weeks, expanding one or two doses in SCLC disease type. This is an open-label multiple dose expansion study.
- Experimental: Part B, Cohort 3 (other c-Kit tumors)NN3201 administered intravenously every three weeks, expanding one or two doses in Other c-Kit tumor disease type. This is an open-label multiple dose expansion study.
Primary Outcome Measure
Number of subjects with Dose-limiting Toxicities: [ Time Frame: 3 weeks ]
Central Contacts
- Clinical Trial Lead1 617.870.7173
Locations (5)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Michigan Hospitals | Ann Arbor | Michigan | 48109-9001 | |
| Case Comprehensive Cancer Center | Cleveland | Ohio | 44106 | Ankit Mangla, MD (216) 844-3951 |
| Oregon Health & Science University | Portland | Oregon | 97239 | |
| The University of Texas MD Anderson Cancer Center | Houston | Texas | 77030 | |
| NEXT Virginia | Fairfax | Virginia | 22031 | - |
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