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A First-in-human Study of the Safety, Pharmacokinetics, Pharmacodynamics and Anti-tumor Activity of SAR439459 Monotherapy and Combination of SAR439459 and Cemiplimab in Patients With Advanced Solid Tumors

Trial Status: Active

Primary Objectives: Dose escalation (Part 1) Part 1A (SAR439459 monotherapy) - To determine the maximum tolerated dose (MTD) and / or maximum administered dose (MAD) of SAR439459 when administered intravenously as monotherapy in adult patients with advanced solid tumors. Part 1B (SAR439459 and cemiplimab combination therapy) - To determine the MTD and / or MAD of SAR439459 administered intravenously in combination with cemiplimab administered intravenously in adult patients with advanced solid tumors. Dose expansion (Part 2) Part 2A (SAR439459 monotherapy) - To determine optimal dose of SAR439459 administered intravenously in adult patients with advanced melanoma who have failed a prior therapy based on anti-PD-1 (programmed cell death-1) or anti-PD-L1. Part 2B (SAR439459 and cemiplimab combination therapy) - To determine the objective response rate (ORR) of SAR439459 in combination with cemiplimab in adult patients with selected advanced solid tumors by evaluation of antitumor response according to Response Evaluation Criteria in Solid Tumors 1.1 (RECIST 1.1). Secondary Objectives: - Pharmacokinetic (PK) profile SAR439459 monotherapy and combined with cemiplimab, PK profile of cemiplimab combined with SAR439459. - Immunogenicity of SAR439459 monotherapy and combined with cemiplimab. Dose escalation (Part 1) - Overall safety / tolerability profile of SAR439459 monotherapy and combined with cemiplimab. - Preliminary recommended phase 2 dose (pRP2D) of SAR439459 as monotherapy or combined with cemiplimab. Dose expansion (Part 2) - Progression free survival (PFS), time to progression (TTP), ORR, and safety of SAR439459 as monotherapy and PFS, TTP, duration of response (DOR), disease control rate (DCR) and safety in combination with cemiplimab. - To confirm the optimal dose of SAR439459 administered in combination with cemiplimab.

Inclusion Criteria

  • Inclusion criteria: Dose escalation (Part 1A and Part 1B) - Patients with histologically confirmed, advanced unresectable or metastatic solid tumor whom in the opinion of the Investigator does not have a suitable alternative therapy. Dose expansion (Part 2A) - Patients with histologically confirmed, advanced unresectable or metastatic melanoma whom in the opinion of the Investigator does not have a suitable alternative therapy. - Patients must have failed a prior therapy based on anti-PD-1 or anti-PD-L1 as defined by disease progression confirmed radiologically within 12 weeks or at the first tumor assessment after commencing treatment without any evidence of a response. - Patients must have a site of disease amenable to biopsy and be a candidate for tumor biopsy. Patients must be able to provide mandatory tumor biopsies prior to and during study treatment. Dose expansion (Part 2B) - Patients with disease location amenable to mandatory tumor biopsy at baseline with histologically confirmed advanced unresectable or metastatic melanoma, colorectal adenocarcinoma, urothelial cancer, hepatocellular carcinoma (HCC), or non-small cell lung cancer (NSCLC). - Melanoma patients must have failed one prior therapy based on anti-PD-1 or anti-PD-L1. - Patients with colorectal cancer must have progressed after last line of therapy. - Patients with urothelial cancer must have disease progression during or following platinum-containing chemotherapy or within 12 months of neoadjuvant or adjuvant treatment with platinum-containing chemotherapy. Patients must not have received >2 lines of therapy for advanced disease. Patients must not have received prior treatment with anti-PD-1 or anti-PD-L1. - Patients with HCC must have failed after 1 prior therapy based on anti-PD-1 or anti-PD-L1. - Patients with NSCLC must have failed after 1 prior therapy based on anti-PD-1 or anti-PD-L1. - Patients with histologically confirmed, advanced unresectable or metastatic melanoma, or colorectal cancer whom in the opinion of the Investigator do not have a suitable alternative therapy. Dose expansion parts 2A and 2B - At least 1 measurable lesion by RECIST v1.1. All cohorts - Patient understands and has signed Informed Consent form and is willing and able to comply with the requirements of the trial. Exclusion criteria: - Age <18 years. - Eastern Cooperative Oncology Group (ECOG) performance status >1. - Concurrent treatment with any other anticancer therapy (including radiotherapy or investigational agents) or participation in another clinical study. - Washout period of less than 3 weeks to prior anticancer therapy. - Women of reproductive potential and male subjects with female partners of childbearing potential who are not willing to avoid pregnancy by using highly effective contraceptive. - Pregnant or breast-feeding women. - Unwillingness and inability to comply with scheduled visits, drug administration plan, laboratory tests, other study procedures, and study restrictions. - Significant and uncontrolled concomitant illness, including any psychiatric condition. - Active infections, including unexplained fever (temperature >38.1ºC), or antibiotic therapy within 1 week prior to enrollment. - Any prior organ transplant including allogeneic bone marrow transplant. - History within the last 5 years of an invasive malignancy other than the one treated in this study, with the exception of resected/ablated basal or squamous-cell carcinoma of the skin or carcinoma in situ of the cervix, or other local tumors considered cured by local treatment. - History of known human immunodeficiency virus (HIV), HIV serology at screening will be conducted only for patients in German study sites. - Known uncontrolled hepatitis B virus (HBV) infection. - Known untreated current hepatitis C virus (HCV) infection. - Any major surgery within the last 28 days. - Patients with primary central nervous system (CNS) tumors and/or CNS metastases of non-CNS primary tumors. - History of congestive heart failure, myocardial infarction with reduced ejection fraction, symptomatic coronary artery disease, documented uncontrolled hypertension, major clinically significant Electrocardiography (ECG) and echocardiogram abnormalities, significant ventricular arrhythmias, significant valvular heart disease (including valve replacement), vascular malformation, aneurysm, significant pulmonary conditions such as idiopathic pulmonary hypertension, uncontrolled chronic lung disease. - History of severe, acute or chronic renal diseases. - Any of the following within 6 months prior to study enrollment: pulmonary embolism, deep vein thrombosis, active uncontrolled bleeding, infectious or inflammatory bowel disease, diverticulitis, intestinal obstruction or perforation and gastrointestinal hemorrhage. - Inadequate hematological, renal or liver function. - Non-resolution of any prior treatment related toxicity to Grade <2. - Prior treatment with any anti-transforming growth factor β (anti-TGFβ) inhibitors. - Known allergies to any component of SAR439459 and/or cemiplimab. - Patients with uveal melanoma and patients with prior or ongoing uveitis. - Patients who received prior immunotherapy who developed toxicity leading to a permanent discontinuation of immunotherapy. - Ongoing or recent (within 5 years) evidence of significant autoimmune disease that required treatment with systemic immunosuppressive treatments. - Immunosuppressive corticosteroid doses (>10 mg prednisone daily or equivalent) within 4 weeks prior to the first dose of SAR439459 and/or cemiplimab (occasional use of inhaled, intraocular, nasal or topical steroids for symptomatic relief allowed). - History of interstitial lung disease or active non-infectious pneumonitis that required immune-suppressive doses of glucocorticoids to assist with management. - Patients with underlying cancer predisposition syndromes. - Receipt of a live vaccine within 30 days of planned start of study medication. - Therapeutic doses of anticoagulants or antiplatelet agents within 7 days prior the first dose of SAR439459. - Prothrombin time (PT) or international normalized ratio (INR) > 1.5 × upper limit of normal (ULN). - Patients accommodated in an institution because of regulatory or legal order; prisoners or patients who are legally institutionalized. The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

California

Duarte
City of Hope Comprehensive Cancer Center
Status: ACTIVE

Kansas

Fairway
University of Kansas Clinical Research Center
Status: ACTIVE
Kansas City
University of Kansas Cancer Center
Status: ACTIVE
Westwood
University of Kansas Hospital-Westwood Cancer Center
Status: ACTIVE

Massachusetts

Boston
Beth Israel Deaconess Medical Center
Status: WITHDRAWN
Brigham and Women's Hospital
Status: ACTIVE
Dana-Farber Cancer Institute
Status: ACTIVE
Massachusetts General Hospital Cancer Center
Status: ACTIVE

North Carolina

Durham
Duke University Medical Center
Status: ACTIVE

The duration of the study for an individual patient will start from the signature of the main informed consent and include a screening period of up to 4 weeks (28 days), a treatment period of at least 1 or 2 cycles (21 or 14 days per cycle, respectively), an end-of-treatment visit at least 30 days following the last administration of study drug (or until the patient receives another anticancer therapy, whichever is earlier), and a follow-up visit 3 months after treatment discontinuation and every 3 months following, until disease progression, or initiation of another antitumor treatment, or death, whichever is earlier. For the urothelial cancer cohort in Part 2B, follow-up visits will occur every 3 months until death or the cutoff date for the overall survival analysis (approximately 12 months after last patient first dose), whichever comes first. Patients who have no disease progression, and continue to benefit from the study drug(s), will be allowed to continue treatment beyond the common study end-date at their assigned dose unless the study is terminated by the Sponsor. The expected enrollment period is approximately 42 months.

Trial Phase Phase I

Trial Type Treatment

Lead Organization
Sanofi Aventis

  • Primary ID TCD14678
  • Secondary IDs NCI-2018-00289, U1111-1187-5425, 2018-001113-32
  • Clinicaltrials.gov ID NCT03192345