Crovalimab History and Updates

34 events · 2016 – present

Synced daily from openFDA and ClinicalTrials.gov. Last sync: .

2
FDA Approvals
0
Label Revisions
32
Trial Milestones
0
Pivotal Publications
Crovalimab — history and updatesFDA approvals, label revisions, recalls, trials, and pivotal publicationsFDA approvalsLabel revisionsRecalls + safetyTrialsPublications20172018201920202021202220232024202520262027202820292030Trial: NCT07172022 2026-03-16 → 2030-03-11 (primary completion)Trial: NCT05494619 2022-11-30 → 2026-03-19 (primary completion)Trial: NCT04912869 2022-03-26 → 2024-12-23 (primary completion)Trial: NCT05075824 2022-03-09 → 2025-06-11 (primary completion)Trial: NCT04958265 2021-11-17 → 2025-07-04 (primary completion)Trial: NCT04861259 2021-10-22 → 2025-10-09 (primary completion)Trial: NCT04654468 2021-03-17 → 2022-02-10 (primary completion)Trial: NCT04434092 2020-10-08 → 2022-11-16 (primary completion)Trial: NCT04432584 2020-09-30 → 2027-09-30 (primary completion)Trial: NCT03157635 2016-11-14 → 2026-09-30 (primary completion)FDA approval — 2024-06-20 FDA approved Piasky (crovalimab) (BLA 761388) Sponsor: GENENTECH INC. Class: Type 1 - New Molecular Entity.FDA approval (supplemental) — 2025-05-14 FDA approved supplemental application for Piasky (crovalimab) — REMS (BLA 761388 S-1) Sponsor: GENENTECH INC. Class: REMS.Results posted — 2023-06-05 Trial results posted: NCT04654468 A Study Evaluating the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Crovalimab in Participants With Paroxysmal Nocturnal HemogResults posted — 2025-11-10 Trial results posted: NCT04434092 A Study Evaluating the Efficacy and Safety of Crovalimab Versus Eculizumab in Participants With Paroxysmal Nocturnal Hemoglobinuria (PNH) Notoday (2026-05-15)FDA approvalLabel revisionRecall or safetyTrial activityPivotal publication

Source: openFDA, ClinicalTrials.gov via AACT, PubMed · Hipa.ai, 2026-05-15Download chart as PNG

This page tracks every FDA action, clinical trial milestone, and major publication for Crovalimab since 2016, drawn from openFDA, ClinicalTrials.gov, and PubMed.

All published updates (5)

Upcoming & expected milestones

Primary completion· ClinicalTrials.gov
Study to Assess Safety, Efficacy, Pharmacokinetics, and Pharmacodynamics of Crovalimab in Healthy Volunteers and Participants With Paroxysma
Primary completion· ClinicalTrials.gov
A Study Evaluating the Safety, Pharmacokinetics, and Efficacy of Crovalimab Versus Eculizumab in Participants With Paroxysmal Nocturnal Hemo

Past events

2026
Primary completion· ClinicalTrials.gov
A Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Crovalimab in Participants With Guillain-Barré Syndrome
2025
Results posted· ClinicalTrials.gov
A Study Evaluating the Efficacy and Safety of Crovalimab Versus Eculizumab in Participants With Paroxysmal Nocturnal Hemoglobinuria (PNH) No
Primary completion· ClinicalTrials.gov
A Study Evaluating the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Crovalimab in Adult and Adolescent Participants With Atypi
Primary completion· ClinicalTrials.gov
A Study Evaluating the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Crovalimab in Pediatric Participants With Atypical Hemolyt
Primary completion· ClinicalTrials.gov
A Study Evaluating the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Crovalimab as Adjunct Treatment in Prevention of Vaso-Occ
2024
Primary completion· ClinicalTrials.gov
A Study Evaluating the Safety, Pharmacokinetics, Pharmacodynamics and Efficacy of Crovalimab for the Management of Acute Uncomplicated Vaso-
2023
Results posted· ClinicalTrials.gov
A Study Evaluating the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Crovalimab in Participants With Paroxysmal Nocturnal Hemog
2022
Trial started· ClinicalTrials.gov
A Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Crovalimab in Participants With Guillain-Barré Syndrome
Primary completion· ClinicalTrials.gov
A Study Evaluating the Efficacy and Safety of Crovalimab Versus Eculizumab in Participants With Paroxysmal Nocturnal Hemoglobinuria (PNH) No
Trial started· ClinicalTrials.gov
A Study Evaluating the Safety, Pharmacokinetics, Pharmacodynamics and Efficacy of Crovalimab for the Management of Acute Uncomplicated Vaso-
Trial started· ClinicalTrials.gov
A Study Evaluating the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Crovalimab as Adjunct Treatment in Prevention of Vaso-Occ
Primary completion· ClinicalTrials.gov
A Study Evaluating the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Crovalimab in Participants With Paroxysmal Nocturnal Hemog
2021
Trial started· ClinicalTrials.gov
A Study Evaluating the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Crovalimab in Pediatric Participants With Atypical Hemolyt
Trial started· ClinicalTrials.gov
A Study Evaluating the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Crovalimab in Adult and Adolescent Participants With Atypi
Trial started· ClinicalTrials.gov
A Study Evaluating the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Crovalimab in Participants With Paroxysmal Nocturnal Hemog
2020
Trial started· ClinicalTrials.gov
A Study Evaluating the Efficacy and Safety of Crovalimab Versus Eculizumab in Participants With Paroxysmal Nocturnal Hemoglobinuria (PNH) No
Trial started· ClinicalTrials.gov
A Study Evaluating the Safety, Pharmacokinetics, and Efficacy of Crovalimab Versus Eculizumab in Participants With Paroxysmal Nocturnal Hemo
2017
2016
Trial started· ClinicalTrials.gov
Study to Assess Safety, Efficacy, Pharmacokinetics, and Pharmacodynamics of Crovalimab in Healthy Volunteers and Participants With Paroxysma

Sources

FDA approvals, label revisions, and recalls come from the public openFDA APIs (Drugs@FDA, Drug Label, Drug Enforcement). Drug-safety communications come from the FDA RSS feed. Trial milestones come from ClinicalTrials.gov via the AACT pg dump. Pivotal-publication events come from PubMed, filtered to high-impact journals linked to a Phase 3 trial in our inventory.