Claudin 18.2-Targeted Chimeric Antigen Receptor T-cells in Subjects With Unresectable, Locally Advanced, or Metastatic Gastric, Gastroesophageal Junction (GEJ), Esophageal, or Pancreatic Adenocarcinoma

Running, not enrolling · Phase 1

Conditions studied: Gastric Cancer, Gastroesophageal-junction Cancer, Esophageal Cancer, Pancreatic Cancer

In brief

This is a Phase 1, Open-Label, Dose Escalation and Expansion, Multicenter Study of Claudin 18.2-Targeted Chimeric Antigen Receptor T-cells in Subjects with Unresectable, Locally Advanced, or Metastatic Gastric, Gastroesophageal Junction (GEJ), Esophageal, or Pancreatic Adenocarcinoma

Key facts

Study ID

NCT05539430

Run by

Legend Biotech USA Inc

People needed

56

Starts

2023-04-18

Expected to finish

2027-12-01

Last updated by the study team

2025-12-12

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• For inclusion in the study, all of the following inclusion criteria must be fulfilled.
• Be willing and able to provide written informed consent.
• Be a female or male ≥ 18 and ≤ 75 years old at the time of signing of the prescreening ICF.
• For Part A and Part B Cohort MR1 only:
• Subjects with histologically/cytologically confirmed unresectable, locally advanced or metastatic adenocarcinoma of the GC/GEJC/EC for which standard treatment is considered intolerable, unlikely to confer significant clinical benefit, is no longer effective, or subject is ineligible or declines standard therapy.
• Subjects must have received prior therapy as follows:
• Previous treatment must have included a fluoropyrimidine and/or platinum containing regimen. Subjects with HER2-neu-positive (HER2+) disease must have also received prior anti-HER2+ therapy.
• Neoadjuvant/adjuvant treatment will be considered as a prior regimen if disease progression occurred during treatment or within 6 months of cessation of treatment.
• For Part B Cohort MR2 only:
• Subjects with histologically/cytologically confirmed unresectable, locally advanced or metastatic PDAC for which standard treatment is considered intolerable, unlikely to confer significant clinical benefit, is no longer effective, or subject is ineligible or declines standard therapy.
• Subjects must have received prior therapy as follows:
• Previous treatment must have included fluoropyrimidine and/or gemcitabine containing regimen.
• Neoadjuvant/adjuvant treatment will be considered as a prior regimen if disease progression occurred during treatment or within 6 months of cessation of treatment.
• For Part B Cohort CR1 only:
• Subjects with histologically/cytologically confirmed metastatic GC/GEJC/EC with RECIST v1.1 SD or PR at the initial response evaluation during first-line SOC treatment.
• Subjects with locally advanced, unresectable disease for whom radiation is not planned may be eligible with Sponsor approval.
• Subjects who develop metachronous metastatic disease after prior (neo)adjuvant treatment for previously localized disease are eligible if at least 6 months have elapsed since completion of prior chemotherapy (and disease status is satisfied, as above).
• Subjects must be clinically suitable to continue at least part of the initial first-line regimen during LB1908 manufacturing.
• Negative for human epidermal growth factor receptor 2 (HER2) or ineligible to receive HER2-directed therapy.
• Subjects must have received prior therapy as follows:
• Acceptable SOC first-line regimens include (but are not limited to) leucovorin/fluorouracil/oxaliplatin (FOLFOX; modifications allowed) and capecitabine/oxaliplatin (CAPOX), with or without an approved immune checkpoint inhibitor.
• Zolbetuximab is allowable as part of first-line SOC (subjects with prior zolbetuximab exposure require Sponsor approval prior to enrollment)
• No investigational therapies in first-line therapy, unless the investigational product is discontinued prior to enrollment on this trial.
• For Part B Cohort CR2 only:
• Subjects with metastatic PDAC with RECIST v1.1 SD or PR at the initial response evaluation during first-line SOC treatment.

You may not qualify if…

• Subjects are not eligible for this study if they fulfill any of the following exclusion criteria:
• Prior treatment with cellular immunotherapy (e.g., CAR-T) or gene therapy product.
• Antitumor therapy prior to Screening as follows (Part A and Part B Monotherapy Regimen [second- or later-line subjects] subjects only):
• Any systemic anticancer therapy (including investigational) within 7 days or at least 5 halflives, whichever is shorter.
• Monoclonal antibody therapy within 2 weeks. Type of monoclonal antibody should be communicated with Sponsor.
• Palliative radiotherapy is permitted with a safety break, the length of which is at the discretion of the Investigator. Radiotherapy directed at sites of disease assessment is also permitted at the discretion of the Investigator and exclusion of the radiated site for disease assessments.
• Unstable/active ulcer, varices, or digestive tract bleeding or recent digestive surgery that may have increased risk of bleeding.
• Clinically significant ascites, pleural or peritoneal effusions requiring weekly clinical intervention at screening.
• Subjects who are on therapeutic anticoagulation. (Note: subjects who are on therapeutic antiplatelet therapy or prophylactic anticoagulation are permitted to participate if deemed to not be at an increased risk of bleeding from their underlying disease or procedures and are required to obtain approval from Sponsor. Similarly, subjects who can have therapeutic anticoagulation de-escalated to prophylactic dosing prior to LB1908 infusion are also eligible).
• Known inherited or acquired immune deficiency without the ability of medical control or normalization.
• History or known brain metastasis or leptomeningeal metastasis. Part B Cohorts MR1 and MR2: Subjects can have brain metastases if previously treated and confirmed stable for at least 4 weeks prior to study entry.
• Subjects with heavy tumor burden such as significant lung disease or extensive liver metastases (e.g., > 5 liver lesions or a single dominant lesion > 5 cm in maximal dimension).
• Active autoimmune disease receiving immunosuppressants (e.g., cyclosporine or high dose systemic steroids) prior to screening as follows:
• Within 2 weeks or 5 half-lives, whichever is longer (those with inhaled or topical steroids recently or currently are not excluded.)
• Immune-related AEs due to prior immune checkpoint therapy must be ≤ Grade 1 with no ongoing immunosuppression, including a systemic steroid dose ≤ 20 mg daily of prednisone equivalent.
• Impaired cardiac function or clinically significant cardiac disease including:
• Unstable angina or myocardial infarction or coronary artery bypass graft (CABG) within 6 months prior to apheresis.
• New York Heart Association (NYHA) Stage III or IV congestive heart failure.
• History of medically uncontrolled clinically significant cardiac arrhythmia (e.g., ventricular tachycardia), complete left bundle branch block, high-grade atrioventricular (AV) block, or third-degree AV block.
• Prior or active malignancy other than the study indication requiring active therapy and/or in the judgment of the Investigator or Sponsor may affect the interpretation of the study endpoints, including the following exceptions:
• Smoldering low grade malignancies may be acceptable as long as the Investigator assesses them of having a significant longer life expectancy than the underlying gastric/pancreatic tumor, after discussion with the Sponsor. Carcinoma in situ.
• Non-melanoma skin cancer (e.g., basal cell or squamous cell carcinoma).
• Serious and/or uncontrolled medical condition that, in the Investigator's judgment, would cause unacceptable safety risk, interfere with study procedures or results, or compromise compliance with the protocol, such as:
• Active, uncontrolled, viral, bacterial, or systemic fungal infection.
• Requirement of supplemental oxygen to maintain oxygen saturation.

Where it is running

• Moffitt Cancer Center — Tampa, Florida, United States
• Karmanos Cancer Institute — Detroit, Michigan, United States
• John Theurer Cancer Center at HackensackUMC — Hackensack, New Jersey, United States
• Roswell Park Comprehensive Cancer Center — Buffalo, New York, United States
• Duke University — Durham, North Carolina, United States
• OHSU Knight Cancer Institute — Portland, Oregon, United States
• Vanderbilt-Ingram Cancer Center — Nashville, Tennessee, United States
• Fred Hutchinson Cancer Center — Seattle, Washington, United States
• Medical College of Wisconsin — Milwaukee, Wisconsin, United States

Full record on ClinicalTrials.gov

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