Condition: Melanoma · Metastatic Melanoma · Advanced Solid Tumor · Sponsor: Replimune, Inc.
This is a noninterventional, observational, long-term follow-up (LTFU) study. Patients in this study will be followed for 5 years from enrollment on this study to assess potential delayed risks of RPx products. Eligible participants for this LTFU study include patients who received at least 1 dose of an RPx product under the interventional parent study. Patients will be rolled over into this LTFU study after completion of the Replimune-sponsored parent study (ie, either completion of the LTFU in the parent study or withdrawal from the parent study). All patients in ongoing RPx studies will be asked to participate in this LTFU study so that the Sponsor can evaluate potential delayed risks.
This description comes directly from the study's public registry record.
Clinical Trials at Replimune · 1-781-222-9570 · Clinicaltrials@replimune.com
Always discuss trial participation with your own doctor first.
| UC San Diego Moores Cancer Center | La Jolla, California, United States | Recruiting |
| Tasman Oncology Research | Southport, Queensland, Australia | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06887348