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FDA Approves Cosibelimab-ipdl for Metastatic or Locally Advanced Cutaneous Squamous Cell Carcinoma

Evidence for efficacy is based on the results from the Study CK-301-101
31 Jan 2025
Immunotherapy
Basal Cell and Squamous Cell Cancers of the Skin

On 13 December 2024, the US Food and Drug Administration (FDA) approved cosibelimab-ipdl (Unloxcyt, Checkpoint Therapeutics, Inc.), a PD-L1 blocking antibody, for adults with metastatic cutaneous squamous cell carcinoma (mCSCC) or locally advanced CSCC (laCSCC) who are not candidates for curative surgery or curative radiation.

Efficacy was evaluated in Study CK-301-101 (NCT03212404), a multicentre, multicohort, open-label trial conducted in 109 patients with mCSCC or laCSCC who were not candidates for curative surgery or curative radiation. Patients were excluded if they had any of the following: active or suspected autoimmune disease, allogeneic transplant within 6 months prior to treatment, prior treatment with anti-PD1/PD-L1 blocking antibodies or other immune checkpoint inhibitor therapy, uncontrolled or significant cardiovascular disease, ECOG performance status ≥ 2, or infection with HIV, hepatitis B, or hepatitis C.

The major efficacy outcome measures were objective response rate (ORR) and duration of response (DoR) as assessed by an independent central review committee (IRC) according to RECIST v1.1. For patients with laCSCC with externally visible target lesions not assessable by radiologic imaging, ORR was determined by ICR assessments of digital photography (WHO criteria). ORR was 47% (95% confidence interval [CI] 36, 59) for 78 patients with mCSCC and 48% (95% CI 30, 67) for 31 patients with laCSCC. Median DoR was not reached (range: 1.4+, 34.1+) in patients with mCSCC and 17.7 months (range: 3.7+, 17.7) in patients with laCSCC.

The most common adverse reactions (≥10%) were fatigue, musculoskeletal pain, rash, diarrhoea, hypothyroidism, constipation, nausea, headache, pruritis, oedema, localised infection, and urinary tract infection.

The recommended cosibelimab-ipdl dose is 1,200 mg administered as an intravenous infusion over 60 minutes every 3 weeks until disease progression or unacceptable toxicity.

This review used the Assessment Aid, a voluntary submission from the applicant to facilitate the FDA’s assessment.

Healthcare professionals should report all serious adverse events suspected to be associated with the use of any medicine and device to FDA’s MedWatch Reporting System.

For assistance with single-patient INDs for investigational oncology products, healthcare professionals may contact FDA’s Oncology Center of Excellence Project Facilitate.

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