Peptide Vaccine To Prevent Acquired Resistance In Patients With Advanced ALK+ NSCLC
Part of paid clinical trials in Baltimore, Maryland.
- Sponsor
- Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
- Study ID
- NCT05950139
- Phase
- PHASE1/PHASE2
- Status
- Recruiting
Conditions
- ALK Fusion Protein Expression
- NSCLC Stage IV
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Peptide vaccine — BIOLOGICALPeptide vaccine
Study Details
The purpose of this study is to evaluate the safety of a cancer peptide vaccine to prevent or delay acquired resistance in advanced ALK+ lung cancer patients currently on ALK targeted therapy.
Key Dates
- Start date
- May 13, 2024
- Status verified
- Sep 2025
- Primary completion
- Jul 31, 2026
- Completion
- Jul 31, 2029
Study Design
- Enrollment
- 12 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Advanced ALK+ NSCLCAll patients will receive the intervention
Primary Outcome Measure
Incidence of treatment-related adverse events [ Time Frame: Up to 2 years ]
Central Contacts
- Vincent Lam, MD410-955-8964
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Johns Hopkins University | Baltimore | Maryland | 21287 | Vincent Lam, MD (PRINCIPAL_INVESTIGATOR) |
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