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Rocket Pharmaceuticals (RCKT) pipeline and stated timing

Pipeline at a glance

ProgramEventStageStated timingFiling
KRESLADI / RP-L201 submission—in 202510-Q ·
marnetegragene autotemcel (KRESLADI) target date (company stated)PDUFAMarch 28, 2026SEC filing ·

Source: ORION, orionbiotechai.com/company/RCKT, data as of Oct 18, 2026
https://www.orionbiotechai.com/company/RCKT

Latest retained statement: marnetegragene autotemcel (KRESLADI) · PDUFA target date (company stated) · March 28, 2026 · SEC filing filed

SEC sources last checked .

Programs and stated timing

○ Quote matched to filing (not yet reviewed by founder) · ✓ Checked by founder.

marnetegragene autotemcel (KRESLADI)

severe leukocyte adhesion deficiency-I

Matched

PDUFA target date (company stated)March 28, 2026

Stage: PDUFASEC filing · “PDUFA) target action date”

Public float: $212,500,000 · as of · SEC filing

Prescription Drug User Fee Act (PDUFA) target action date for March 28, 2026

SEC filing · Filed · Last checked

Source details

Accession 0001140361-26-006981

Resolution filing: · SEC filing

How this date was described over time

Company periods and sentences are quoted as written. A matching disclosure uses the SEC filing date for the same program and event type. As of .

Program / eventStated period and SEC wordingDisclosure in stated period
marnetegragene autotemcel (KRESLADI)FDA decisionMarch 28, 2026
“Prescription Drug User Fee Act (PDUFA) target action date for March 28, 2026”

Filed · SEC original

Not compared

The stated period has ended. ORION has no record of a complete search of SEC filings from that period.

marnetegragene autotemcel (KRESLADI)FDA decisionMarch 28, 2026
“PDUFA date of March 28, 2026”

Filed · SEC original

Not compared

The stated period has ended. ORION has no record of a complete search of SEC filings from that period.

marnetegragene autotemcel (KRESLADI)FDA decisionMarch 28, 2026
“PDUFA date of March 28, 2026”

Filed · SEC original

Not compared

The stated period has ended. ORION has no record of a complete search of SEC filings from that period.

marnetegragene autotemcel (KRESLADI)FDA decisionMarch 28, 2026
“PDUFA date set by the FDA is March 28, 2026”

Filed · SEC original

Not compared

The stated period has ended. ORION has no record of a complete search of SEC filings from that period.

marnetegragene autotemcel (KRESLADI)FDA decisionMarch 28, 2026
“PDUFA date set by the FDA is March 28, 2026”

Filed · SEC original

Not compared

The stated period has ended. ORION has no record of a complete search of SEC filings from that period.

KRESLADI / RP-L201Submissionin 2025
“Submission of a complete BLA to resolve CRL is anticipated in 2025.”

Filed · 10-Q

Not compared

The stated period has ended. ORION has no record of a complete search of SEC filings from that period.

KRESLADI / RP-L201Submissionbefore the end of 2025
“submission of complete BLA to resolve Complete Response Letter is anticipated before the end of 2025.”

Filed · EX-99.1

Not compared

ORION has no confirmed start and end dates for this wording, so it is not compared with filings.

KRESLADI / RP-L201Submissionin 2025
“Submission of complete BLA to resolve Complete Response Letter anticipated in 2025.”

Filed · EX-99.1

Not compared

The stated period has ended. ORION has no record of a complete search of SEC filings from that period.

KRESLADI / RP-L201Submissionin 2025
“Submission of a complete BLA to resolve the CRL is anticipated in 2025.”

Filed · 10-Q

Not compared

The stated period has ended. ORION has no record of a complete search of SEC filings from that period.

KRESLADI / RP-L201Submissionin 2025
“Submission of a complete BLA to resolve CRL is anticipated in 2025.”

Filed · 10-Q

Not compared

The stated period has ended. ORION has no record of a complete search of SEC filings from that period.

KRESLADI / RP-L201Submissionin 2025
“Submission of complete BLA to resolve Complete Response Letter anticipated in 2025.”

Filed · EX-99.1

Not compared

The stated period has ended. ORION has no record of a complete search of SEC filings from that period.

KRESLADI / RP-L201Submissionin 2025
“Submission of complete BLA to resolve Complete Response Letter anticipated in 2025.”

Filed · 10-K

Not compared

The stated period has ended. ORION has no record of a complete search of SEC filings from that period.

“Not compared” means ORION has not matched this wording against a complete set of SEC filings for its period. It says nothing either way about whether a matching filing exists. Wording without exact dates is not given calendar dates.

Retained company announcements

Historical summaries and source dates are retained separately from the SEC timing quotes above. Earlier publications were collected retrospectively.

Historical catalog checked .

No historical announcement trail is retained for this company in this catalog.

Selected registry record

RP-A701 is a recombinant viral vector composed of an AAV serotype rh.74 (AAVrh.74) capsid encapsulating the transgene, BCL2-associated Athanogene 3 (BAG3) · NCT07137338

Condition in the selected registry record
Dilated Cardiomyopathy (DCM)
Phase in the selected registry record
Phase 1
Identity checked

Original ClinicalTrials.gov record · Open the selected study

Retained company–study identity sources

Scope of retained company and registry evidence

These are selected linked records and dated source metadata, not a live registry recheck or the company’s full pipeline. Company announcements and the selected registry study are separate evidence sets. No stage or event timing is borrowed between them.

Coverage and identity checks

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Reading these records

First stated window
The timing wording in the earliest company statement located within the sources checked, quoted as written (for example “2H 2026”). An earlier statement may exist outside those sources.
Disclosure date
The date of the filing or company release that disclosed the readout. “None found” means no such disclosure was located in the sources checked. SEC filings were searched through the “SEC filings searched through” date shown.
1H, 2H, 1Q–4Q
First or second half, or first to fourth quarter, of the year named, as the company wrote it. Equivalent notations are compared together; the original wording stays visible.
SEC original
The filing as published on the SEC EDGAR system. “Company original” is the release on the company's own investor site.
Status
One of seven labels set by founder review of the original filings. Definitions: Methodology.

See RCKT in the calendar · Review labels and methodology

A New Drug Application (NDA) or Biologics License Application (BLA) asks the FDA to approve a drug or biologic for sale.A PDUFA date is the target date by which the FDA aims to decide on a drug or biologic application.