XTX202 in Patients With Advanced Solid Tumors
About the study
A First-in-Human, Multicenter, Phase 1/2, Open-Label Study of XTX202 in Patients with Advanced Solid Tumors
Who can take part
You may be eligible to participate in the study if you meet the following criteria:
INCLUSION CRITERIA
Inclusion Criteria:
Disease Criteria
- Phase 1, Part 1a: Any histologically or cytologically confirmed solid tumor malignancy that is locally advanced or metastatic and has failed standard therapy, or standard therapy is not curative or available
- Phase 1, Part 1b: Histologically or cytologically confirmed solid tumor malignancy with one of the following tumor histologies: RCC of clear cell histology only, melanoma, squamous cell skin carcinoma, ovarian cancer, non-small cell lung cancer. Those patients who previously received immunotherapy must have derived benefit from this treatment. Additionally, patients with any of the above histologies in an advanced setting who plan to undergo debulking surgery or oligometastasectomy may be eligible to receive 2 cycles of XTX202 treatment in a "window of opportunity" subcohort".
- Phase 2, Part 2a: Patients with metastatic RCC who have previously been treated with an anti-PD-1 and a TKI, per local and institutional SOC. Patients must have progressed on treatment with an anti-PD-1 mAb administered either as monotherapy or in combination with other therapies
- Phase 2, Part 2b: Patients with unresectable or metastatic melanoma who have previously been treated with at least 1 prior line of therapy in the recurrent or metastatic setting. Prior therapy must have included an anti-PD-1 alone or in combination per local and institutional standard of care, and patient must have progressed on checkpoint inhibitor therapy. Patients with BRAF V600-activating mutation must have previously received targeted therapy per local and institutional standard of care.
- ECOG performance status of 0 or 1
- Adequate organ function
- Part 1b only patients must be willing to provide fresh tumor biopsies before and after initiation of study treatment.
EXCLUSION CRITERIA
Exclusion Criteria:
- Received prior treatment with IL-2 therapy
- History of clinically significant pulmonary disease
- History of clinically significant cardiovascular disease
- Has a diagnosis of immunodeficiency
- Has an active autoimmune disease that has required systemic treatment in past 2 years, including the use of disease modifying agents, corticosteroids or immunosuppressive drugs
- Has an active infection requiring systemic therapy within 4 weeks prior to study treatment
Study Locations
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How to Apply
Contact the study center to learn if this study is a good match for you.
Study’s details
Contition
Advanced Solid Tumor
Age (in years)
18+
Phase
Phase 1/Phase 2
Participants needed
189
Est. Completion Date
Apr 30, 2024
Treatment type
Interventional
Sponsor
Xilio Development, Inc.
ClinicalTrials.gov identifier
NCT05052268
Study number
XTX202-01/02-001
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