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Prelude Therapeutics annual meeting: all director nominees elected, auditor ratified, say-on-pay approved
Elected Krishna Vaddi, Paul Scherer, Katina Dorton as Class III directors with over 26.9M shares for each.
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Prelude Therapeutics Q1 net loss $10.4M ($0.13/sh); cash runway into Q2 2028 after $90M offering
Net loss of $10.4M ($0.13 per share) vs $32.1M ($0.42) in Q1 2025; R&D spend fell to $13.6M.
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Prelude Therapeutics prices $90M public offering of common stock and pre-funded warrants
Offering of 18,018,014 common shares at $4.44/share and pre-funded warrants for 2,252,252 shares at $4.4399.
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Prelude Therapeutics presents preclinical data for PRT13722 KAT6A degrader at AACR 2026, plans IND mid-2026
PRT13722 is a first-in-class, orally bioavailable, potent and highly selective KAT6A degrader for HR+/HER2- breast cancer.
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Prelude Therapeutics appoints Dr. Charles Q. Morris as Chief Medical Officer effective April 20, 2026
Dr. Morris, age 61, brings over 30 years of oncology drug development experience; most recently CMO at Lava Therapeutics.
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Prelude Therapeutics files $25M ATM equity offering via Jefferies
Filed prospectus supplement to sell up to $25M common stock under existing Sales Agreement with Jefferies LLC.
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Prelude Therapeutics FY2025 net loss narrows to $99.5M; cash $106.4M; IND cleared for PRT12396
Net loss of $99.5M ($1.29/share) improved from $127.2M ($1.68/share) in 2024.
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FDA clears IND for Prelude's JAK2V617F inhibitor PRT12396; Phase 1 to start by Q2 2026
FDA cleared IND for PRT12396, a mutant-selective JAK2V617F inhibitor for myeloproliferative neoplasms.
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Prelude Therapeutics furnishes investor presentation; no material new information disclosed
Filed an investor presentation dated January 2026 for use in investor meetings starting Jan 9.
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Prelude Q3 net loss $19.7M; cash into 2027; JAK2/KAT6A IND timelines set
Q3 net loss $19.7M ($0.26/sh) vs $32.3M ($0.43) YoY; cash $58.2M at Sep 30.
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Prelude gets $60M from Incyte for JAK2V617F option; pauses SMARCA2; CMO resigns
Incyte receives exclusive option to acquire Prelude's mutant selective JAK2V617F JH2 inhibitor program for $100M exercise price, plus up to $775M milestones and single-digit royalties.
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Prelude Therapeutics appoints Katina Dorton to board; Mardi Dier resigns
Mardi Dier resigned as Class III director effective Oct 17, 2025, not due to any disagreement.
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Prelude Therapeutics regains Nasdaq minimum bid price compliance as of Sept 18, 2025
Received Nasdaq non-compliance notice on March 27, 2025 for failing $1.00 bid price requirement.
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Prelude Therapeutics Q2 net loss $31.2M; pauses IV SMARCA2 degrader, focuses on oral PRT7732
Net loss of $31.2M ($0.41 per share) improved from $34.7M ($0.46) in Q2 2024.
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Prelude Therapeutics appoints new director from Baker Bros.; shareholders approve increase in authorized shares
Appointed Paul Scherer, M.D. (Baker Bros. Advisors) as Class III director; granted options for 76,000 shares vesting over one year.
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Prelude Q1 2025 net loss $32.1M; cash $103.1M funds ops into Q2 2026
Cash, cash equivalents, restricted cash and marketable securities of $103.1M as of March 31, 2025.
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Prelude Therapeutics presents preclinical data on SMARCA2 and KAT6A degraders at AACR
PRT3789, a selective SMARCA2 degrader in Phase 1/2, shows deep SMARCA2 degradation and high selectivity over SMARCA4.
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Prelude Therapeutics receives Nasdaq bid price deficiency notice; has until Sep 23, 2025 to cure
Nasdaq notified Prelude on March 27, 2025 that its common stock closed below $1.00 for 30 consecutive business days.
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Prelude Therapeutics FY2024 net loss $127.2M; cash runway into Q2 2026
Net loss $127.2M ($1.68/share) vs $121.8M ($2.02/share) in FY2023; R&D expense rose to $118.0M.
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Prelude Therapeutics appoints Bryant D. Lim as permanent CFO; base salary $483K
Bryant D. Lim, previously interim CFO, appointed permanent CFO effective Feb 3, 2025; retains roles of Chief Legal Officer and Corporate Secretary.
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Prelude Therapeutics reports interim Phase 1 data for PRT2527; plans to partner CDK9 program
PRT2527 monotherapy ORR 17.4% (4/23 evaluable); combination with zanubrutinib ORR 38.5% (5/13 evaluable).
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Prelude Therapeutics Q3 net loss $32.3M; PRT3789 shows partial responses in SMARCA4-mutated cancers
Cash, equivalents and marketable securities $153.6M; net loss $32.3M ($0.43/share) vs $30.6M prior year.
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Prelude Therapeutics PRT3789 Phase 1 interim data: 4 PRs; DAC program preclinical proof-of-concept
Interim Phase 1 results: 4 confirmed partial responses (2 esophageal, 2 NSCLC) out of 26 evaluable SMARCA4 loss-of-function patients.
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Prelude reports Phase 1 interim data: PRT3789 shows 3 confirmed PRs in NSCLC/esophageal, well tolerated
3 confirmed partial responses in 2 esophageal and 1 NSCLC patient out of 26 evaluable; 7 patients had tumor shrinkage.
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Prelude Therapeutics Publishes Phase 1 Abstract for PRT3789 SMARCA2 Degrader at ESMO 2024
Abstract details first clinical data for PRT3789, a first-in-class IV SMARCA2 degrader in SMARCA4-mutated advanced solid tumors.
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Prelude Therapeutics Q2 net loss $34.7M; cash $179.8M; clinical milestones for SMARCA2 and CDK9 programs
Net loss $34.7M ($0.46/share) vs $30.4M ($0.54/share) in Q2 2023; R&D expense rose to $29.5M from $25.0M.
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Prelude Therapeutics stockholders elect two Class I directors, ratify EY as auditor
Paul A. Friedman, M.D. elected as Class I director with 31,165,370 votes for, 1,762,716 withheld.
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Prelude Therapeutics posts corporate presentation and SMARCA degrader educational series
Company furnished a corporate presentation (Exhibit 99.1) dated June 2024.
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Prelude Therapeutics grants 25,000 stock options to Interim CFO Bryant D. Lim
Options to purchase 25,000 shares of common stock at $3.86 per share.
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Prelude Therapeutics Q1 net loss $31.4M; cash $201.9M; pipeline on track for H2 2024 data
Net loss $31.4M ($0.42/diluted share) vs $27.7M ($0.58) in Q1 2023; R&D spend $27.4M up from $21.8M.
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Prelude Therapeutics CFO departs; Bryant Lim named interim CFO
Laurent Chardonnet ceased as CFO on April 8, 2024; he will consult at $500/hr through Oct 4, 2024.
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Prelude Therapeutics reports FY2023 net loss of $121.8M; cash runway into 2026, pipeline milestones set for 2024
Cash and marketable securities $232.9M as of Dec 31, 2023, expected to fund operations into 2026.
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Prelude Therapeutics raises $25M via pre-funded warrant private placement for SMARCA2 pipeline
Gross proceeds ~$25M from sale of 7,936,759 pre-funded warrants at $3.1499 each, exercise price $0.0001.
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Prelude prioritizes SMARCA2 and CDK9, partners with AbCellera on ADCs, reports Q3 net loss $30.6M
Q3 net loss $30.6M ($0.45/share); cash at $230.5M; cash runway into 2026.
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Prelude posts Q2 net loss $30.4M; cash $255M funds operations into 2026
Net loss of $30.4M ($0.54/share) vs $27.4M ($0.58/share) in Q2 2022.
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Prelude Therapeutics shareholders elect two Class III directors, ratify auditor, approve charter amendment
Krishna Vaddi, Ph.D. and Mardi C. Dier elected as Class III directors with ~27M votes for each.
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Prelude Therapeutics furnishes May 2023 investor presentation
Company prepared investor presentation materials for use in investor meetings.
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Prelude Therapeutics prices $100M public offering of common stock and pre-funded warrants
Offering of 3.05M voting shares and 1.45M non-voting shares at $5.75/share; pre-funded warrants for 12.9M shares at $5.7499 each.
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Prelude Therapeutics files updated investor presentation; no material new data disclosed
Company filed an updated corporate presentation dated May 2023 as Exhibit 99.1 to Form 8-K.
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Prelude Therapeutics Q1 2023 net loss $27.7M; cash runway unchanged into Q4 2024
Net loss $27.7M ($0.58 loss per share) vs $29.5M ($0.63) in Q1 2022.
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Prelude Therapeutics reports FY 2022 net loss of $115.4M; cash runway through Q4 2024
Net loss of $115.4M ($2.44 per share) vs $111.7M ($2.43 per share) in FY 2021.
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Prelude Therapeutics enters $75M at-the-market stock offering agreement with Jefferies
Company entered Open Market Sale Agreement with Jefferies LLC to sell up to $75M of common stock.
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Prelude Therapeutics posts investor presentation for SVB Global Biopharma Conference
Filed investor presentation under Regulation FD for Feb 2023 SVB conference.
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Prelude Therapeutics amends bylaws for universal proxy rules and DGCL updates
Amended bylaws effective Jan 19, 2023, addressing SEC universal proxy rules (Rule 14a-19) and recent DGCL amendments.
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Prelude Therapeutics files corporate presentation; no specific new details provided
Prelude Therapeutics made a corporate presentation available to investors on January 9, 2023.
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Prelude Q3 net loss $30.0M; FDA clears two INDs, halts PRMT5 internal development
Net loss of $30.0M ($0.63 per share) vs $30.7M ($0.66) in Q3 2021.
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Prelude Therapeutics Q2 2022 net loss $27.4M; cash $246.3M; IND accepted for CDK4/6 inhibitor PRT3645
Net loss $27.4M ($0.58/share) vs $26.9M ($0.58/share) Q2 2021; R&D declined $1.1M to $21.3M.
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Prelude Therapeutics stockholders elect three Class II directors and ratify auditor at 2022 annual meeting
Martin Babler elected with 27,034,110 votes for; 54,875 withheld; 1,215,046 broker non-votes.
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Prelude Q1 net loss $29.5M ($0.63/sh); cash $266.2M funds into 2H2024; on track for data readouts in 2H2022
Net loss $29.5M ($0.63/sh) vs $21.3M ($0.47) YoY; R&D expense $22.8M ($16.5M) on increased clinical activity.
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Prelude Therapeutics EVP/Chief of Clinical Affairs Morosini resigns; advisor through May 5
Deborah Morosini resigned as EVP and Chief of Clinical Affairs effective April 6, 2022.