BLAINTRAVENOUSINJECTABLE
Approved
Jun 2024
Lifecycle
Growth
Competitive Pressure
30/100
Clinical Trials
10
Data completeness
4/8 — Partial
PIASKY (crovalimab) by Roche is complement c5 inhibitors [moa]. Approved for complement c5 inhibitor [epc]. First approved in 2024.
Drug data last refreshed 2h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
PIASKY (crovalimab) is a monoclonal antibody complement C5 inhibitor approved in June 2024 for treating complement-mediated diseases. It works by blocking the C5 protein in the complement cascade, preventing inflammatory cell damage. The drug is administered intravenously and represents a new mechanism in complement inhibition therapy.
Growth
Early-stage growth asset from Roche with emerging market presence; commercial teams are likely expanding to support market penetration and indication expansion.
Mechanism of Action
Complement C5 Inhibitors
Pharmacologic Class:
Complement C5 Inhibitor
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (10)
A Study to Evaluate Crovalimab in People With Antiphospholipid Syndrome (APS)
Started Mar 2026
0Antiphospholipid Syndrome
A Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Crovalimab in Participants With Guillain-Barré Syndrome (GBS)
Started Nov 2022
0Guillain-Barré Syndrome
A Study Evaluating the Safety, Pharmacokinetics, Pharmacodynamics and Efficacy of Crovalimab for the Management of Acute Uncomplicated Vaso-Occlusive Episodes (VOE) in Participants With Sickle Cell Disease (SCD).
Started Mar 2022
30 enrolled
Sickle Cell Disease
A Study Evaluating the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Crovalimab as Adjunct Treatment in Prevention of Vaso-Occlusive Episodes (VOE) in Sickle Cell Disease (SCD)
Started Mar 2022
95 enrolled
Sickle Cell Disease
A Study Evaluating the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Crovalimab in Pediatric Participants With Atypical Hemolytic Uremic Syndrome (aHUS)
Started Nov 2021
41 enrolled
Atypical Hemolytic Uremic Syndrome
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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.