TrialPath
← Back to searchRecruiting

A Phase 1/2 Study to Evaluate CHM-2101, an Autologous Cadherin 17 Chimeric Antigen Receptor (CAR) T Cell Therapy

NCT06055439 · Chimeric Therapeutics
In plain English

Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.

Official title
A Phase 1/2 Study to Evaluate CHM-2101, an Autologous Cadherin 17 (CDH17) Chimeric Antigen Receptor (CAR) T Cell Therapy for the Treatment of Relapsed or Refractory Gastrointestinal Cancers
About this study
This is a Phase 1/2 open-label study to evaluate CHM-2101, an autologous CDH17 CAR T-cell therapy for the treatment of advanced gastrointestinal (GI) cancers that are relapsed or refractory to at least 1 standard treatment regimen in the metastatic or locally advanced setting. The study has 2 parts: Phase 1, Dose Escalation and Expansion, and Phase 2. Potential participants will provide written consent and be screened for study eligibility prior to undergoing any screening procedures, including leukapheresis. Protocol-specified criteria must be met prior to the start of leukapheresis for collection of peripheral blood mononuclear cells (PBMCs). Eligible participants will undergo leukapheresis to collect PBMCs for product manufacturing, which comprises enrichment of T cells, lentiviral transduction, ex vivo expansion, and cryopreservation of the CHM-2101 cell product. Participants who have a leukapheresis or manufacturing failure may be permitted a second attempt at leukapheresis. Bridging chemotherapy (treatment between the time of leukapheresis and first dose of lymphodepleting chemotherapy \[LDC\]) is permitted at the discretion of the investigator, if needed to maintain disease stability during CHM-2101 manufacturing time. Bridging chemotherapy is prohibited within the 2 weeks prior to leukapheresis and 2 weeks prior to planned CHM-2101 infusion. Specific criteria to proceed should be reviewed prior to leukapheresis, LDC, and CHM-2101 infusion. Participants will be followed in this study for 18 months or until disease progression.
Eligibility criteria
Inclusion Criteria: 1. Documented informed consent of the participant and/or legally authorized representative. 2. Confirmed histologic diagnosis of one of the following solid tumors of GI origin: 1. Gastric adenocarcinoma Note: for gastric adenocarcinoma patients only, central laboratory confirmation of CDH17+ tumor expression is required. 2. Colon and/or rectal adenocarcinoma 3. G1, G2, and well-differentiated G3 neuroendocrine tumors of the midgut and hindgut (ileal, jejunal, cecal, distal colonic, or rectal; with ≤ 55% Ki67 expression) 3. Availability of unstained tumor tissue slides from archived tumor tissue or a new tumor biopsy, if medically feasible. Note: for gastric adenocarcinoma patients only, confirmation of CDH17+ is required prior to study inclusion. 4. Have received at least 1 prior line of systemic anti-cancer treatment in the locally advanced or metastatic setting, as defined by National Comprehensive Cancer Network (NCCN) guidelines. Participants must have received or declined FDA-approved and available treatment options, including targeted therapies for disease mutation or antigen expression status. 5. Age ≥ 18 years and ≤ 85 years. 6. For Phase 1 Dose Expansion and Phase 2 only: Measurable disease as per RECIST v1.1 criteria (Note: Measurable disease is NOT required for Phase 1 Dose Escalation). 7. Eastern Cooperative Oncology Group (ECOG) ≤ 1. 8. Life expectancy ≥ 12 weeks. 9. No known contraindications to leukapheresis, cyclophosphamide, fludarabine, or steroids. 10. Baseline laboratory values as shown in the following table: Minimum Laboratory Values for Study Entry Laboratory Assessment Criteria White blood cell count \> 4,000/mm3 Absolute neutrophil count (ANC) ≥ 1,500/mm3 Platelets ≥ 100,000/mm3 Hemoglobin ≥ 10 g/dL Total bilirubin ≤ 1.5 x upper limit of normal (ULN) Aspartate amino transferase (AST) ≤ 3 x ULN Alanine transaminase (ALT) ≤ 3 x ULN Creatinine clearance by Cockroft-Gault equation 60 mL/min Oxygen saturation ≥ 92% on room air Albumin ≥ 3 g/dL 11. Left ventricular ejection fraction ≥ 50%. 12. Seronegative for human immunodeficiency virus (HIV) by antigen/antibody (Ag/Ab) testing. 13. Seronegative for hepatitis B and/or hepatitis C virus. 14. Women of childbearing potential (WOCBP) must have a negative urine or serum pregnancy test. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test is required. 15. Agreement by women and men of childbearing potential to use an effective method of birth control or abstain from heterosexual activity through at least 3 months after the last dose of CHM-2101. Exclusion Criteria: 1. Previous treatment with CDH17-targeted therapies. 2. Unresolved toxicities from prior therapy except for chronic toxicity no greater than Grade 1 and stable \> 30 days (Note: alopecia of any grade is not exclusionary). 3. Uncontrolled seizure activity and/or known central nervous system (CNS) metastases. 4. History of allergic reactions attributed to compounds of similar chemical or biologic composition to study agent. 5. Uncontrolled Crohn's disease, ulcerative colitis, or other autoimmune or inflammatory disorders of the GI tract. "Uncontrolled" is defined as requiring hospitalization, corticosteroids, or chronic medication increase (dosage or frequency) within the previous 6 months. 6. Liver involvement ≥ 50%. 7. Active infection requiring oral or IV antibiotics. 8. Current diagnosis of pleural effusions, interstitial lung disease, or heart failure of New York Heart Association Classification of Heart Failure Class III or IV. 9. Ongoing treatment with systemic corticosteroid therapy at doses of prednisone ≥ 20 mg/day or equivalent (lower doses of corticosteroid therapy are allowed until 7 days prior to leukapheresis). 10. No prior malignancy within 5 years except for non-melanomatous skin cancer or cervical cancer treated with curative intent 11. Currently breastfeeding or planning to become pregnant within 9 months of study enrollment. 12. Any other clinically significant uncontrolled illness or other comorbid condition that would, in the investigator's judgment, contraindicate the participant's participation in the clinical study.
Study design
Enrollment target: 135 participants
Allocation: na
Masking: none
Age groups: adult, older_adult
Timeline
Starts: 2024-05-15
Estimated completion: 2027-05
Last updated: 2026-01-29
Interventions
Biological: CHM-2101 CAR-T cells
Primary outcomes
  • Dose-Limiting Toxicity (DLT) (28 Days)
  • Rates and Grades of Cytokine Release Syndrome (CRS) (up to 15 years)
  • All other adverse events and toxicities (up to 15 years)
Sponsor
Chimeric Therapeutics · industry
Contacts & investigators
ContactChimeric Clinical · contact · clinical@chimerictherapeutics.com · (323) 366-9009
InvestigatorJennifer Eads, MD · principal_investigator, University of Pennsylvania
All locations (4)
Emory UniversityRecruiting
Atlanta, Georgia, United States
University of ChicagoRecruiting
Chicago, Illinois, United States
University of PennsylvaniaRecruiting
Philadelphia, Pennsylvania, United States
Sarah Cannon Research InstituteRecruiting
Nashville, Tennessee, United States
A Phase 1/2 Study to Evaluate CHM-2101, an Autologous Cadherin 17 Chimeric Antigen Receptor (CAR) T Cell Therapy · TrialPath