# Rocket Pharmaceuticals Announces FDA Acceptance of BLA Resubmission of KRESLADI™ for the Treatment of Severe Leukocyte Adhesion Deficiency-I (LAD-I)
Canonical URL: https://biopharmsignal.com/news/RCKT/rocket-pharmaceuticals-announces-fda-acceptance-of-bla-resubmission-of-kresladitm-for-the-treatment-of-severe-leukocyte-adhesion-deficiency-i-lad-i
Ticker: RCKT
Company: Rocket Pharmaceuticals
Source: Rocket Pharmaceuticals
Published: 2025-10-14 11:00 EST
Original Source URL: https://ir.rocketpharma.com
## Summary

Prescription Drug User Fee Act (PDUFA) target action date is March 28, 2026 All primary and secondary endpoints were met, and KRESLADI™ was well tolerated Rocket is eligible for a Rare Pediatric Disease Priority Review Voucher, should KRESLADI ™ be approved CRANBURY, N.J. --(BUSINESS WIRE)--Oct.

## Article Body
Prescription Drug User Fee Act (PDUFA) target action date is March 28, 2026 All primary and secondary endpoints were met, and KRESLADI™ was well tolerated Rocket is eligible for a Rare Pediatric Disease Priority Review Voucher, should KRESLADI ™ be approved CRANBURY, N.J. --(BUSINESS WIRE)--Oct.
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- 2026-03-27 11:00 EST — [Rocket Pharmaceuticals Announces FDA Approval of KRESLADI™ for Pediatric Patients with Severe Leukocyte Adhesion Deficiency-I (LAD-I)](https://biopharmsignal.com/news/RCKT/rocket-pharmaceuticals-announces-fda-approval-of-kresladitm-for-pediatric-patients-with-severe-leukocyte-adhesion-deficiency-i-lad-i) — Source: Rocket Pharmaceuticals
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