NCT06398418
Recruiting
Phase 1
A Single and Repeat Dosing and Expansion Study of the Safety, Drug Exposure and Clinical Activity of R-5780 in Combination With a PD-1 (Checkpoint Protein on Immune Cells Called T Cells) Pathway Checkpoint Inhibitor in Patients With Solid Tumors
Overview
- Phase
- Phase 1
- Intervention
- R-5780
- Conditions
- Solid Tumor, Adult
- Sponsor
- Rise Therapeutics LLC
- Enrollment
- 33
- Locations
- 1
- Primary Endpoint
- Incidence and severity of adverse events and their relationship to R-5780 (probiotic) administration
- Status
- Recruiting
- Last Updated
- 8 months ago
Overview
Brief Summary
The goal of this study is determine the safety and tolerability of orally taken probiotic (R-5780) in patients currently on a PD-1 Pathway Checkpoint Inhibitor (checkpoint protein on immune cells called T cells) with Solid Tumors.
Detailed Description
Patients will take an oral dosage of probiotic (R-5780 and provide patient reported overall feeling and physician scored measure of their tumors. Blood and fecal evaluations of inflammation and assessment of probiotic (R-5780) on fecal levels will also be measured.
Investigators
Eligibility Criteria
Inclusion Criteria
- •At least 18 years of age to 80
- •Ability to provide written informed consent
- •Unresectable stage III or stage IV melanoma, basal cell carcinoma, or squamous cell carcinoma as per the American Joint Committee on Cancer 2017 Guidelines (8th Edition) regardless of BRAF mutation status and other solid tumors.
- •Refractory to anti-PD (checkpoint Protein on Immune Cells called T cells)-1/L1 therapy per RECIST v1.1 defined as subject who has disease progression after receiving at least two complete cycles of ICI (immune checkpoint inhibitors) therapy or disease progression 6 months from initiation of ICI (immune checkpoint inhibitors) therapy while still on active therapy.
- •Life expectancy of greater than 3 months
- •Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1 or 2
- •Subjects must have evaluable disease by CT (computer tomography) or MRI (magnet resonance imaging) per RECIST 1.1 criteria or clinically apparent disease that the investigator can follow for response.
Exclusion Criteria
- •Any serious medical condition or laboratory abnormality or psychiatric condition or any other significant or unstable concurrent medical illness (in the opinion of the Investigator) would preclude protocol adherence or would make the safety of the study drug difficult to assess
- •Treatment with systemic broad-spectrum antibiotics.
- •No active viral infections.
- •Coexisting severe chronic diseases other than cancer (autoimmunity, inflammatory diseases)
- •Secondary gastrointestinal motility disorders
- •History of solid organ transplant or bone marrow transplant
- •Prior CAR-T (chimeric antigen receptor) or allogeneic cellular therapy
- •Ongoing systemic immunosuppressive therapy, with the exclusion of prednisone (10 mg/day)
- •Concurrent therapy with any other investigational agent, vaccine, or device
- •Pregnant or breastfeeding or planning to conceive or father a child during the trial period
Arms & Interventions
Open Label
R-5780 Probiotic
Intervention: R-5780
Outcomes
Primary Outcomes
Incidence and severity of adverse events and their relationship to R-5780 (probiotic) administration
Time Frame: Baseline through Week 4
To assess the number of participants with treatment-related adverse events after taking R-5780 (probiotic)
Secondary Outcomes
- Scale (QOLS)(Baseline through End of Study Day 112)
Study Sites (1)
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