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Fulcrum to merge with Slate Medicines; Slate holders to own ~95% of combined company
Merger values Slate at $350M, Fulcrum at $31.3M; post-close ownership: Slate holders ~55.9%, investors ~39.1%, Fulcrum ~5.0%.
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Fulcrum approves retention bonuses for CEO, CLO, CFO; accounting officer departs after restructuring
CEO Alex Sapir receives $370,040 retention bonus; CLO Curtis Oltmans $195,480; CFO Alan Musso $195,200.
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Fulcrum cuts workforce 85% after SCD drug failure; hires Leerink for strategic review
Workforce reduced from 57 to 9 employees (~85% cut) after discontinuing pociredir for sickle cell disease.
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Fulcrum Therapeutics discontinues pociredir program in SCD; initiates strategic review
Discontinued pociredir for sickle cell disease after FDA feedback; no viable regulatory path forward.
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Fulcrum Therapeutics Q1 net loss $18.9M, CFO retiring, CAMP4 license terminated, pociredir trial planned H2 2026
CFO Alan Musso retiring; will stay until successor named then consultant through Feb 2027.
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Fulcrum Therapeutics Q4/FY2025: positive pociredir Phase 1b HbF data; net loss widens to $74.9M
Positive 12-week pociredir Phase 1b results: mean absolute HbF increased 12.2% (7.1% to 19.3%); improvements in hemolysis, anemia, and VOC trends.
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Fulcrum reports ~$352.3M cash as of Dec 31, 2025; updates presentation for JPM conference
Preliminary unaudited cash, cash equivalents and marketable securities of $352.3M as of December 31, 2025.
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Fulcrum Therapeutics prices $175M upsized public offering of common stock and pre-funded warrants
Priced underwritten offering of 11,851,853 shares at $13.50/share and pre-funded warrants for 1,111,193 shares at $13.499 each.
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Fulcrum reports positive Phase 1b data for pociredir in SCD: 58% patients achieved HbF>=20% at 20 mg dose
Mean absolute HbF increased 9.9% at Week 6 in 20 mg cohort (vs 5.6% in 12 mg); 7 of 12 patients (58%) achieved HbF ≥20%.
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Fulcrum Therapeutics Q3 loss $19.6M; pociredir 20mg cohort enrolled, data due year-end
Cash, equivalents and marketable securities $200.6M; cash runway into 2028.
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Fulcrum Q2 net loss $17.3M; pociredir Phase 1b shows HbF increase 8.6% in SCD
Q2 2025 net loss $17.3M vs net income $55.4M in Q2 2024; cash $214.1M, runway into 2028.
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Fulcrum Q1 net loss $17.7M; pociredir 12mg cohort enrolled, 20mg cohort initiated
Net loss of $17.7M for Q1 2025 vs $26.9M in Q1 2024; cash $226.6M at March 31, 2025.
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MyoKardia terminates Fulcrum collaboration; Fulcrum loses future milestones and royalties
MyoKardia (BMS unit) terminated the collaboration agreement for convenience; effective June 26, 2025.
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Fulcrum Therapeutics reports Q4 2024 net loss $16.6M; cash $241M, runway into at least 2027
Full-year 2024 net loss $9.7M vs $97.3M in 2023, driven by $80M Sanofi upfront payment.
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Sanofi terminates losmapimod deal; Fulcrum loses up to $975M in milestones
Sanofi terminated for convenience the May 2024 collaboration for losmapimod (FSHD) effective April 17, 2025.
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Fulcrum Therapeutics Q3 net loss $21.7M, cash $257.2M; losmapimod halted, PIONEER trial ongoing
Net loss $21.7M in Q3 2024 vs $24.0M loss in Q3 2023; R&D expenses down to $14.6M from $18.2M.
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Fulcrum Therapeutics reduces workforce from 80 to 51, expects $10M annual savings
Workforce reduction of 29 employees (36%) to focus on pociredir, DBA, and early discovery; suspends losmapimod.
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Fulcrum Therapeutics Phase 3 losmapimod trial fails; program suspended
REACH trial missed primary endpoint: RSA change p=0.75 vs placebo at week 48.
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Fulcrum Therapeutics exchanges 9.35M shares for pre-funded warrants with RA Capital and another stockholder
RA Capital exchanged 8,500,000 shares for a pre-funded warrant for 8,500,000 shares at $0.001 exercise price, no expiration.
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Fulcrum Therapeutics reports Q2 net income of $55.4M, on track for Phase 3 FSHD data by Oct 2024
Net income $55.4M vs net loss $23.8M in Q2 2023; revenue $80M from Sanofi upfront payment.
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Fulcrum signs $80M upfront Sanofi deal for losmapimod ex-U.S.; Q1 net loss $26.9M
Sanofi pays $80M upfront; Fulcrum eligible for up to $975M in milestones and tiered low-teens to mid-twenties royalties on ex-U.S. sales.
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Fulcrum Therapeutics Q4 2023 net loss $24.8M; Phase 3 REACH data expected Q4 2024
Net loss $24.8M in Q4 2023 (vs $26.1M); full-year net loss $97.3M (vs $109.9M).
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Fulcrum Therapeutics Q3 2023: net loss $24M, Phase 3 enrollment complete, cash runway extended into 2026
Completed enrollment in Phase 3 REACH trial of losmapimod for FSHD; topline data expected Q4 2024.
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Fulcrum Therapeutics announces FDA lifts clinical hold on FTX-6058 IND for sickle cell disease
FDA lifted clinical hold on Fulcrum's IND for FTX-6058 on August 22, 2023.
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Fulcrum Therapeutics reports Q2 net loss $23.8M, closes FSHD trial screening, appoints CFO
Net loss of $23.8M in Q2 2023, improved from $34.1M in Q2 2022; cash $278.2M.
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Fulcrum licenses CAMP4's Diamond Blackfan Anemia program for up to $70M in milestones plus royalties
Exclusive worldwide license to CAMP4's DBA program, including small molecule compounds and patent rights.
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Fulcrum Therapeutics appoints Alex Sapir CEO, reports Q1 net loss of $24.8M, FTX-6058 on clinical hold
Alex Sapir appointed CEO/President effective July 1, 2023; he will serve as special advisor until then.
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Fulcrum Therapeutics CFO Esther Rajavelu resigns effective April 21, 2023
CFO Esther Rajavelu resigns effective April 21, 2023 to pursue another opportunity.
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FDA places FTX-6058 on clinical hold; Fulcrum reports Q4/FY2022 results
FDA placed full clinical hold on FTX-6058 IND for sickle cell disease; enrollment paused and dosing suspended.
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Fulcrum Therapeutics prices upsized public offering of 9.6M shares at $13.00, expected gross proceeds of $125M
Offered 9,615,384 shares at $13.00 per share; gross proceeds of $125 million.
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Fulcrum announces $100M stock offering and preliminary $202.9M cash position
Preliminary cash, cash equivalents, and marketable securities of ~$202.9M as of Dec 31, 2022.
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CEO transition and positive FTX-6058 Phase 1b data; cash runway into late 2024
CEO Bryan Stuart departs; Robert Gould, former CEO/board member, appointed interim CEO effective Jan 3, 2023.
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Fulcrum Therapeutics Q3 net loss $23.7M; cash $221.8M; selected 12mg dose for FTX-6058 SCD trial
Net loss $23.7M vs $20.7M year ago; collaboration revenue fell to $1.2M from $4.9M due to Acceleron wind-down.
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Fulcrum Therapeutics announces $75M public offering of common stock at $7.82/share
9,590,792 shares offered at $7.82/share; gross proceeds $75 million.
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Fulcrum Therapeutics Q2 net loss $34.1M; cuts 18 jobs, saves $40-50M, cash into mid-2024
Net loss $34.1M ($0.65 per share) vs $19.6M in Q2 2021; cash $169M as of June 30.
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Fulcrum reports positive Phase 1b data for FTX-6058 in sickle cell disease; HbF up 6.3%
FTX-6058 achieved up to 6.3% increase in fetal hemoglobin (HbF) over baseline in Phase 1b trial.