BLAINJECTIONINJECTABLE
Approved
Dec 2024
Lifecycle
Growth
Competitive Pressure
30/100
Clinical Trials
4
Data completeness
3/8 — Basic
UNLOXCYT (cosibelimab) by Checkpoint Surgical is programmed death ligand-1 antagonists [moa]. First approved in 2024.
Drug data last refreshed 6h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
UNLOXCYT (cosibelimab) is a programmed death ligand-1 (PD-L1) antagonist monoclonal antibody administered by injection. It works by blocking PD-L1, thereby unleashing T-cell-mediated immune responses against tumor cells. The drug was approved in December 2024 and represents a checkpoint inhibitor entering a competitive oncology landscape.
Growth
Early-stage launch phase with significant room for market penetration; commercial teams are building infrastructure for ramp-up.
Mechanism of Action
Programmed Death Ligand-1 Antagonists
Pharmacologic Class:
Programmed Death Ligand-1 Blocker
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (4)
Cosibelimab for CSCC in Patients With Kidney Transplant or Hematologic Malignancy
Started Jul 2026
80 enrolled
Cutaneous Squamous Cell CarcinomaSkin Cancer
Study of Pemetrexed+Platinum Chemotherapy With or Without Cosibelimab in First Line Metastatic Non-squamous NSCLC
Started Dec 2021
25 enrolled
Metastatic Non-squamous Non Small Cell Lung Cancer
Study of Cosibelimab in Subjects With Relapsed or Refractory Lymphoma
Started Apr 2019
18 enrolled
B-cell Non Hodgkin LymphomaRichter's Transformation
Phase 1 Study of CK-301 (Cosibelimab) as a Single Agent in Subjects With Advanced Cancers
Started Sep 2017
272 enrolled
Lung NeoplasmsCarcinoma, Non-Small-Cell LungCarcinoma, Small Cell+10 more
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.