CI

At a glance

ClinicalIndex Comparison Record
Phase 3Active· 51 enrolled / 51 target
Drug / intervention
PF-06838435/ fidanacogene elaparvovecbiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03861273
NCT03861273Phase 3ActiveUpdate Overdue (0.6/mo)Completion was 43mo ago

Phase 3, Open-label, Single-arm Study to Evaluate Efficacy and Safety of FIX Gene Transfer With PF-06838435 (rAAV-Spark100-hFIX-R338L) in Adult Male Participants With Moderately Severe to Severe Hemophilia B (FIX:C ≤2%) (BeneGene-2)

Pfizer·interventional·Posted Mar 4, 2019·Updated Jun 1, 2026

In Brief

A Phase 3 clinical trial evaluating PF-06838435/ fidanacogene elaparvovec for Hemophilia B. Active but no longer recruiting, targeting 51 participants across 67 sites in 16 countries.

Signals

Enrollment appears stalled

Detailed Summary

This study will evaluate the efficacy and safety of PF-06838435 (a gene therapy drug) in adult male participants with moderately severe to severe hemophilia B (participants that have a Factor IX circulating activity of 2% or less). The gene therapy is designed to introduce genetic material into cells to compensate for missing or non-functioning Factor IX. Eligible study participants will have completed a minimum 6 months of routine Factor IX prophylaxis therapy during the lead in study (C0371004). Participants will be dosed once (intravenously) and will be evaluated over the course of 6 years. The main objective of the study will evaluate the annualized bleeding rate \[ABR\] for participants treated with gene therapy versus standard of care (SOC) therapy (FIX prophylaxis replacement regimen).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHemophilia B
CountriesAustralia, Brazil, Canada, France, Germany, Greece, Italy, Japan, Saudi Arabia, South Korea, Spain, Sweden, Taiwan, Turkey (Türkiye), United Kingdom, United States
Collaborators--

Timeline

Phase 3Active
2019202020212022202320242025202620272028202920302031
First PostedMar 4, 2019
Enrollment StartJul 29, 2019
Primary CompletionNov 16, 2022
Study CompletionFeb 25, 2031
TodayJul 2, 2026
Enrollment to primary: 3.3 yearsPosted 7.3 years ago

Arms & Interventions

PF-06838435/ fidanacogene elaparvovecexperimental

Biological: PF-06838435/ fidanacogene elaparvovec

Interventions

PF-06838435/ fidanacogene elaparvovecbiological

Gene Therapy