Neoplasm Malignant Clinical Trial
Official title:
A First-in-human Phase 1 Dose Escalation Study of SAR428926 in Patients With Advanced Solid Tumors
Primary Objectives:
To determine the maximum tolerated dose (MTD) of SAR428926 when administered as a single
agent in patients with advanced solid tumors.
To evaluate the anti-tumor response of SAR428926 when administered as a single agent in
patients with advanced triple negative breast cancer (TNBC) positive for the protein targeted
by SAR428926 To assess the preliminary anti-tumor response of SAR428926 when administered as
a single agent in patients with advanced solid tumors positive for the protein targeted by
SAR428926
Secondary Objectives:
To determine the overall safety profile of SAR428926 as a single agent. To characterize the
pharmacokinetics (PK) profile of SAR428926 and its metabolites.
To identify the recommended Phase 2 dose (RP2D) of SAR428926 as a single agent. To evaluate
the immunogenicity of SAR428926. To assess the tumor response and duration of tumor response
in all treated patients.
To evaluate the benefit of primary prophylaxis on the occurrence of corneal
(keratopathy/keratitis) toxicity (Expansion cohorts).
The study duration for an individual patient will include a screening period for inclusion of up to 28 days, a treatment period, an end-of-treatment (EOT) visit around 30 days following the last administration of SAR428926, and at least one follow-up visit around 30 days after the EOT visit. The treatment period may continue until disease progression, intolerable toxicity, or investigator, Sponsor, or patient decision to discontinue therapy. Patients who discontinue treatment for reasons other than progression of disease will be followed every 3 months until progression, initiation of subsequent therapy, or until the primary analysis cutoff date, whichever comes first. ;
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