CAR-macrophages for the Treatment of HER2 Overexpressing Solid Tumors (NCT04660929) | Clinical Trial Compass
UnknownPhase 1
CAR-macrophages for the Treatment of HER2 Overexpressing Solid Tumors
United States48 participantsStarted 2021-02-02
Plain-language summary
Phase 1, first-in-human, open label study of CAR macrophages in HER2 overexpressing solid tumors.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* HER2-positive recurrent or metastatic solid tumors for which there are no available curative treatment options.
* Breast cancer and gastric/gastroesophageal junction cancers must have failed approved HER2-targeted agents.
* Other HER2-positive tumor types must have failed standard of care therapies, while prior therapy with anti-HER2 drugs is not required.
* Subject must be willing and able to undergo tumor tissue biopsy procedures
* Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
* Subject has adequate bone marrow and organ function
Exclusion Criteria:
* HIV, active hepatitis B or hepatitis C infection.
* Diagnosis of immunodeficiency or chronic exposure to systemic corticosteroid therapy or any other form of immunosuppressive therapy
* Untreated or symptomatic central nervous system (CNS) metastases or cytology proven carcinomatous meningitis.
o Subjects with small, asymptomatic CNS metastases that do not require treatment are permitted to enroll.
* Left ventricular ejection fraction (LVEF) \<50% as determined by ECHO or multiple gated acquisition scan (MUGA)
Other protocol-defined Inclusion/Exclusion may apply.
CT-0508 in Combination with Pembrolizumab Substudy Only:
Exclusion Criteria:
* Subjects with severe hypersensitivity (≥Grade 3) to pembrolizumab and/or any of its excipients
* Subjects with an active autoimmune disease that has required systemic treatment in past 2 years (i.e., with use of disease modifying ag…
What they're measuring
1
Assess the safety and tolerability of CT-0508 by estimating the frequency and severity of adverse events in subjects with HER2 overexpressing solid tumors.
Timeframe: 14 months
2
Assess the feasibility of manufacturing CT-0508 by describing the percentage of products passing release criteria.
Timeframe: 12 months
3
Assess the safety and tolerability of CT-0508 in combination with pembrolizumab by estimating the frequency and severity of adverse events in subjects with HER2 overexpressing solid tumors (CT-0508 and pembrolizumab substudy only)