Ruxolitinib for Cancer Cachexia
Part of paid clinical trials in Dallas, Texas.
- Sponsor
- Tu Dan
- Study ID
- NCT04906746
- Phase
- EARLY_PHASE1
- Status
- Active Not Recruiting
Conditions
- Cachexia
- Stage IV Non-small Cell Lung Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Identify any dose-limiting toxicity (DLT) when ruxolitinib is administered to NSCLC cachexia patients. — DRUGThere will be intra-patient dose escalation of ruxolitinib in every patient enrolled on study.
Study Details
To assess toxicity with use of Ruxolitinib in NSCLC cachexia patients; to associate levels of JAK/STAT signaling in blood, adipose, and muscle pre- and post-ruxolitinib treatment with changes in cachexia and anorexia.
Key Dates
- Start date
- Feb 23, 2022
- Status verified
- Jul 2025
- Primary completion
- Sep 27, 2024
- Completion
- Dec 31, 2025
Study Design
- Enrollment
- 10 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Dosing Regimen for RuxolitinibLevel 0: Ruxolitinib 0 MG po bid for 1 month (Month 1) Level 1: Ruxolitinib 10 MG po bid for 1 month (Month 2) Level 2: Ruxolitinib 15 MG po bid for 1 month (Month 3)
Primary Outcome Measure
Number of non-small cell lung cancer cachexia patients with toxicity with the use of Ruxolitinib [ Time Frame: 3 months ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| UT Southwestern Medical Center | Dallas | Texas | 75390 | - |
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