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Approved For Marketing EXPANDED_ACCESS NCT03154437

An Expanded Access Program of Emicizumab in Participants With Hemophilia A With Inhibitors

An Open-Label, Multicenter, Expanded Access Program for Emicizumab in Patients With Hemophilia A With Inhibitors

Sponsor: Genentech, Inc.

Conditions Hemophilia A
Interventions Emicizumab
Updated 7 times since 2017 Last updated: Mar 26, 2018
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

This observational or N/A phase trial investigates Hemophilia A and is currently ongoing. Genentech, Inc. leads this study, which shows 7 recorded versions since 2026 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.

Status Flow

~Jun 2017 – ~Aug 2017 · 2 months · monthly snapshotAvailable~Aug 2017 – ~Apr 2018 · 8 months · monthly snapshotAvailable~Apr 2018 – ~Jun 2018 · 2 months · monthly snapshotApproved For Marketing~Jun 2018 – ~Jan 2021 · 31 months · monthly snapshotApproved For Marketing~Jan 2021 – ~Jul 2024 · 42 months · monthly snapshotApproved For Marketing~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshotApproved For Marketing~Sep 2024 – present · 24 months · monthly snapshotApproved For Marketing

Change History

7 versions recorded
  1. Sep 2024 — Present [monthly]

    Approved For Marketing

  2. Jul 2024 — Sep 2024 [monthly]

    Approved For Marketing

  3. Jan 2021 — Jul 2024 [monthly]

    Approved For Marketing

  4. Jun 2018 — Jan 2021 [monthly]

    Approved For Marketing

  5. Apr 2018 — Jun 2018 [monthly]

    Approved For Marketing

    Status: AvailableApproved For Marketing · Phase: NANone

Show 2 earlier versions
  1. Aug 2017 — Apr 2018 [monthly]

    Available NA

  2. Jun 2017 — Aug 2017 [monthly]

    Available NA

    First recorded

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Genentech, Inc.
Data source: Genentech, Inc.

For direct contact, visit the study record on ClinicalTrials.gov .