Moderate hemophilia A

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At a Glance

Live from database

Regulatory Watchboard

9 events
Jul 2024Canadian CHO-KLAT/H-FIT Study - Quality of Life of, and Burden of Caring for, Persons With Hemophilia

The Hospital for Sick Children

TrialNOT YET RECRUITING
Aug 2023Prevention of Bleeding in Patients With Moderate and Severe Hemophilia A Playing Sports: A Comparison Between Factor VIII and Emicizumab Prophylaxis

Wayne State University

TrialRECRUITING
Jun 2023

ROCTAVIAN: FDA approved

treatment of adults with severe hemophilia A (congenital factor VIII deficiency with factor VIII activity less than 1 IU/dL) without antibodies to adeno-associated virus serotype 5 (AAV5) detected by an FDA-approved test

FDAcompleted
Aug 2022ASC618 Gene Therapy in Hemophilia A Patients

ASC Therapeutics — PHASE1, PHASE2

TrialRECRUITING
Jun 2022A Study to Evaluate Overall Health, Physical Activity, and Joint Outcomes in Participants With Severe or Moderate Hemophilia A Without Factor VIII Inhibitors on Emicizumab Prophylaxis

Hoffmann-La Roche — PHASE4

TrialACTIVE NOT RECRUITING
Nov 2017

Hemlibra: FDA approved

Routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adult and pediatric patients with hemophilia A (congenital factor VIII deficiency) with factor VIII inhibitors

FDAcompleted
Jun 2014

Eloctate: FDA approved

Indicated in adults and children with Hemophilia A (congenital Factor VIII deficiency) for on-demand treatment and control of bleeding episodes, perioperative management of bleeding, and routine prophylaxis to reduce the frequency of bleeding episodes.

FDAcompleted
Dec 2013

TRETTEN: FDA approved

Routine prophylaxis of bleeding in patients with congenital Factor XIII A-subunit deficiency.

FDAcompleted
Feb 2011

Corifact: FDA approved

For the routine prophylactic treatment of congenital factor XIII deficiency

FDAcompleted

Data from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.

Financial Assistance

5 programs

FINANCIAL LANDSCAPE SUMMARY

5

Total programs

5

Open now

3

Copay cards

Copay Assistance3

Eloctate

Bioverativ Therapeutics, Inc.

OpenContact for details

Corifact

CSL Behring LLC

OpenContact for details

TRETTEN

Novo Nordisk, Inc.

OpenContact for details

Patient Assistance Programs2

Hemlibra

Genentech, Inc.

OpenContact for detailsApply ↗

ROCTAVIAN

BioMarin Pharmaceutical Inc.

OpenContact for detailsApply ↗

View all support programs on disease page →

Approved Treatments

5 FDA-approved

ROCTAVIAN

(VALOCTOCOGENE ROXAPARVOVEC-RVOX)Orphan drug

BioMarin Pharmaceutical Inc.

Approved Jun 2023FDA label ↗

Hemlibra

(EMICIZUMAB)Orphan drug

Genentech, Inc.

Approved Nov 2017FDA label ↗

Eloctate

(antihemophilic factor (recombinant), Fc fusion protein)Orphan drug

Bioverativ Therapeutics, Inc.

Approved Jun 2014

TRETTEN

(coagulation factor XIII A-subunit (recombinant))Orphan drug

Novo Nordisk, Inc.

Approved Dec 2013

Corifact

(factor XIII concentrate (human))Orphan drug

CSL Behring LLC

Approved Feb 2011

View full treatment details on disease page →

Clinical Trial Landscape

3 active trials
1Phase 4
1Unknown
1PHASE1, PHASE2
3Total recruiting
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Recent News & Research

1 article
FDAOct 25, 2025

Hemlibra Expanded Indication Approved for All Hemophilia A

FDA approved expanded indication for Hemlibra covering all severity levels regardless of inhibitor status.

Read ↗

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Specialist Network

Top 6 by expertise

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