RPTR-168 in Patients With Human Papillomavirus Strain 16 (HPV-16) E6/E7 Positive Tumors and Melanoma
Recruiting in Palo Alto (17 mi)
+3 other locations
Age: 18+
Sex: Any
Travel: May Be Covered
Time Reimbursement: Varies
Trial Phase: Phase 1
Waitlist Available
Sponsor: Repertoire Immune Medicines
No Placebo Group
Trial Summary
What is the purpose of this trial?
This trial tests a new drug, RPTR-168, to see if it is safe for patients with certain types of cancer that haven't responded to other treatments. The drug is given through an IV to see if it can help fight the cancer cells.
Research Team
DS
David Spriggs, MD
Principal Investigator
Repertoire Immune Medicines
Eligibility Criteria
Inclusion Criteria
Failure to respond to standard therapy, or for whom no appropriate therapies are available (based on the judgment of the Investigator).
Tumor refractory to or progressing following prior PD-1/PD-L1 therapy alone or in combination with an anti-CTLA-4 agent unless the patient was deemed ineligible for such treatment.
If a subject is BRAF V600E/K positive, they must have received an approved BRAF- targeted regimen prior to entering the study, unless the patient was deemed ineligible for such treatment.
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Treatment Details
Interventions
- RPTR-168 (Virus Therapy)
Participant Groups
1Treatment groups
Experimental Treatment
Group I: RPTR-168Experimental Treatment1 Intervention
Escalating doses of RPTR-168 as a monotherapy in HPV-16 E6/E7 positive tumors and melanoma.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Repertoire Immune Medicines
Lead Sponsor
Trials
3
Recruited
50+