A Study of CM24 in Combination with Nivolumab in Adults with Advanced Solid Tumors

Completed · Phase 1/Phase 2

Conditions studied: Solid Tumor, Non Small Cell Lung Cancer, Pancreatic Cancer, Ovarian Cancer, Papillary Thyroid Cancer, Melanoma, Colorectal Adenocarcinoma

In brief

This is an open-label, multicenter, multi-dose escalation and dose expansion study in subjects with selected advanced solid tumors (Part A) and advanced metastatic pancreatic cancer (Parts C \& D) to evaluate the safety and tolerability of CM-24 in combination with nivolumab. In Part C of the study gemcitabine/nab-paclitaxel or Nal-IRI/5-FU/LV will be administered subsequent to CM24 and nivolumab. CM24, nivolumab and gemcitabine/nab-paclitaxel or Nal-IRI/5-FU/LV are administered intravenously.

Key facts

Study ID

NCT04731467

Run by

Famewave Ltd.

People needed

79

Starts

2021-03-19

Expected to finish

2024-09-30

Last updated by the study team

2024-12-27

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Part A: Previously treated subjects with recurrent and/or metastatic NSCLC, pancreatic cancer, ovarian cancer, papillary thyroid cancer, colorectal adenocarcinoma and melanoma with documented progression/intolerance following at least one previous therapy (and not more than 2 previous regimens); Part C: Subjects with histologically confirmed advanced metastatic pancreatic adenocarcinoma as defined by NCCN Guidelines; Subjects with islet cell neoplasms are excluded; subjects with a maximum of 1 prior treatment regimen for metastatic disease excluding: nab-paclitaxel containing regimens and up to 8 weeks from last chemotherapy treatment (Arm #1); fluoropyrimidine or irinotecan containing regimens and up to 8 weeks from last chemotherapy treatment (Arm #2).
• Part C, D: Subjects with histologically confirmed advanced metastatic pancreatic adenocarcinoma as defined by NCCN Guidelines; Subjects with islet cell neoplasms are excluded.
• Parts C, D: Subjects who have progressed on or after standard of care chemotherapy with a maximum of 1 prior treatment regimen for advanced metastatic disease:
• Subjects enrolled in arm with gemcitabine/nab-paclitaxel combination should have received a fluoropyrimidine and/or irinotecan containing regimen in the first line of treatment; Prior gemcitabine containing regimen may be allowed only if completed at least 6 months prior to study enrollment.
• Arm #2: Subjects enrolled in arm with Nal-IRI/5FU/LV combination should have received a gemcitabine and/or nab-paclitaxel containing regimen in the first line of treatment; Prior irinotecan and/or fluoropyrimidine containing regimens may be allowed only if completed at least 6 months prior to study enrollment.
• Part A: Availability of an archival tumor sample prior to first treatment. Parts C, D: Fresh tumor biopsy must be obtained within 3 months prior to enrollment and after the last systemic treatment was completed.
• Must have at least 1 measurable lesion per RECIST1.1 with progressing or new tumors since last antitumor therapy;
• ECOG performance status score of 0 or 1;
• Adequate safety lab results;
• Stable brain metastases;
• WCBP (Women of Childbearing Potential) must have a negative serum pregnancy test at Screening and a negative urine pregnancy test, WCBP must agree to abstain from sex or use an adequate method of contraception, males must abstain from sex with WCBP or use an adequate method of contraception.

You may not qualify if…

• Part A: Received more than two prior systemic regimens for the metastatic disease Parts C and D: Received more than 1 prior systemic regimens for the advanced metastatic disease
• Part A: History of weight loss >10% over the 2 months prior to Screening;
• Unresolved AEs > Grade 1 from prior anticancer therapy.
• Concurrent malignancy requiring treatment;
• Active, untreated central nervous system (CNS) metastases;
• Subjects previously treated with an anti PD-1/PD-L1 targeting agent with history immune mediated toxicity;
• Severely immunocompromised;
• History of allergy or hypersensitivity to any of the study treatment components;
• Major surgery within 4 weeks of study administration;
• Received a live / attenuated vaccine within 30 days of first treatment
• Clinically relevant serious co-morbid medical conditions including, but not limited to:
• Active infection;
• Recent (within six months of Screening) cardiac disease, myocardial infarction, or severe or unstable angina;
• History of serious arrhythmia;
• Chronic obstructive or chronic restrictive pulmonary disease, pulmonary hypertension history of or active interstitial lung disease or pneumonitis;
• Prior organ allograft;
• Subjects with active, known or suspected autoimmune disease;
• History of active or latent tuberculosis infection;
• Positive test for HIV, HBV, or HCV;
• Radiation within two weeks prior to the first study treatment;
• Treatment with another investigational therapy within 30 days or 5 half-lives of the drug prior to Screening, whichever is longer;
• Treatment with botanical preparations (e.g., herbal supplements or traditional Chinese medicines) intended for general health support or to treat the disease under study within 2 weeks prior to treatment;
• Pregnant or lactating women.

Where it is running

• HonorHealth Research Institute — Scottsdale, Arizona, United States
• University of Colorado — Aurora, Colorado, United States
• Yale University — New Haven, Connecticut, United States
• Barbara Ann Karmanos Cancer Institute — Detroit, Michigan, United States
• The University of Texas M.D. Anderson Cancer Center — Houston, Texas, United States
• Rambam Health Care Campus — Haifa, Israel
• Sheba Medical Center — Ramat Gan, Israel
• Hospital Clinic Barcelona — Barcelona, Spain
• NEXT Oncology Barcelona — Barcelona, Spain
• Vall d' Hebron Institute of Oncology (VHIO) — Barcelona, Spain
• Clinica Universidad de Navarra — Madrid, Spain
• Hospital 12 Octubre — Madrid, Spain
• Hospital General Universitario Gregorio Maranon — Madrid, Spain
• Hospital South Texas Accelerated Research Therapeutics (START) Madrid - CIOCC — Madrid, Spain
• South Texas Accelerated Research Therapeutics (START) Madrid - Hospital Fundacion Jimenez Diaz — Madrid, Spain
• Clinica Universidad de Navarra - Pamplona — Pamplona, Spain
• NEXT Oncology Madrid — Pozuelo de Alarcón, Spain
• Hospital Quiron Salud Valencia — Valencia, Spain

Full record on ClinicalTrials.gov

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