RCKT
Rocket Pharmaceuticals, Inc.3.4300
+0.0200+0.59%
Dec 16, 4:00:00 PM EST
Earnings Call Transcripts
This Quarter (Q1 '26)
No earnings call transcript available yet
Last Quarter (Q4 '25)
No earnings call transcript available
Key Stats
Market Cap
371.20MP/E (TTM)
-Basic EPS (TTM)
-2.25Dividend Yield
0%Recent Filings
10-K
FY2025 results
Rocket posted FY2025 net loss of $223.1M, improved from $258.7M in 2024, on $142.0M R&D (down 17%) and $86.5M G&A (down 15%), fueled by 30% workforce cut slashing opEx 25%. Q4 momentum centered on BLA resubmission for KRESLADI (PDUFA Mar 2026) post-CRL and FDA lifting Phase 2 hold for RP-A501 after SAEs traced to C3 inhibitor. Restructuring prioritizes AAV cardio programs, de-emphasizing FA/PKD. Cash at $188.9M funds into Q2 2027. Clinical holds disrupt trials.
8-K
Q4 results, $189M cash
Rocket Pharmaceuticals reported Q4 and full-year 2025 results on February 26, 2026, posting a net loss of $223.1M, down from $258.7M in 2024, with R&D expenses dropping to $142.0M from $171.2M amid cost controls. Cash stands at $188.9M, funding operations into Q2 2027. KRESLADI™ awaits FDA decision March 28; Danon trial resumes 1H26. Pipeline advances briskly.
8-K
Q3 loss narrows; pipeline advances
Rocket Pharmaceuticals reported Q3 2025 net loss of $50.3M, down from $66.7M year-over-year, with R&D expenses dropping to $34.1M and G&A to $18.4M amid restructuring. Cash stands at $222.8M, funding operations into Q2 2027. FDA lifted hold on RP-A501 Danon trial; KRESLADI PDUFA set for March 28, 2026. New C-suite bolsters commercialization push.
10-Q
Q3 FY2025 results
Rocket Pharmaceuticals narrowed its Q3 operating loss to $52.2M from $69.4M y/y, while YTD loss improved to $187.8M from $210.5M, thanks to R&D cuts from $42.3M to $34.1M and G&A from $27.1M to $18.4M amid a July 2025 workforce reduction of 30% that charged $3.3M YTD. Cash burn slowed, with operating cash use at $155.2M YTD versus $162.8M prior, leaving $222.8M in cash and investments to fund into Q2 2027. Restructuring trimmed direct program costs across Danon disease and others. FDA lifted a Phase 2 hold on RP-A501 in August. Securities litigation lingers.
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