Melanoma Clinical Trial

Exercise to Boost Response to Checkpoint Blockade Immunotherapy

Summary

30 minutes of moderate exercise on an arm ergometer, a cycle ergometer, or a treadmill prior to each administration of standard of care checkpoint blockade immunotherapy across all cycles

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:
Age ≥ 18 years
Able to read and speak English fluently
Capable of giving informed consent
Reported ability to complete 20-30 minutes moderate exercise per positive response to "can you currently walk unaided for six minutes or more?".
Scheduled for first-time checkpoint blockade immunotherapy with FDA-approved drugs, including avelumab, cemiplimab, ipilimumab, nivolumab, pembrolizumab or relatlimab in the absence of other therapies (e.g. targeted therapy)
Melanoma patients (adjuvant setting)
Melanoma patients (neoadjuvant setting)
cuSCC patients (neoadjuvant setting)
Merkel cell carcinoma patients (neoadjuvant setting)

Participants may also be required to have a full COVID vaccination series; the most up-to-date best practice guidelines for research at Moffitt Cancer Center will dictate the need for such a vaccination series.

Exclusion Criteria:

Presence of medical conditions, such as severe cardiovascular disease for which an exercise intervention may not be warranted.
Presence of major postoperative complications for which an exercise intervention may not be warranted.

Study is for people with:

Melanoma

Phase:

Early Phase 1

Estimated Enrollment:

32

Study ID:

NCT05358938

Recruitment Status:

Recruiting

Sponsor:

H. Lee Moffitt Cancer Center and Research Institute

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There is 1 Location for this study

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Moffitt Cancer Center
Tampa Florida, 33612, United States More Info
Stephanie Forgas
Contact
813-745-5734
[email protected]
Peter Kanetsky, PhD, MPH
Principal Investigator
Vernon K Sondak, MD
Sub-Investigator
Ahmad A Tarhini, MD, PhD
Sub-Investigator

How clear is this clinincal trial information?

Study is for people with:

Melanoma

Phase:

Early Phase 1

Estimated Enrollment:

32

Study ID:

NCT05358938

Recruitment Status:

Recruiting

Sponsor:


H. Lee Moffitt Cancer Center and Research Institute

How clear is this clinincal trial information?

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