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Allogene shareholders approve doubling authorized shares to 800M; files $135M ATM offering
Stockholders approved increase of authorized common shares from 400M to 800M, effective June 18, 2026.
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Allogene appoints Zachary Roberts as CEO effective July 1, 2026; David Chang becomes non-employee director
Zachary Roberts, M.D., Ph.D., currently EVP R&D and CMO, named President and CEO effective July 1, 2026.
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Allogene Q1 net loss $42.6M; ALPHA3 interim shows 58% MRD clearance; cash runway extended to Q1 2029
Terminated exclusive license with Overland; retains ~3% equity; no termination payments.
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Allogene prices $175M public offering of 87.5M shares at $2.00 per share
Offering of 87,500,000 shares at $2.00/share; gross proceeds ~$175M before discounts and expenses.
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Allogene's cema-cel shows 41.6% MRD clearance advantage in ALPHA3 Phase 2 interim
58.3% (7/12) of cema-cel patients achieved MRD negativity vs 16.7% (2/12) in observation arm.
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Allogene Therapeutics launches underwritten public offering, suspends ATM sales
Company announced proposed underwritten public offering of common stock on April 13, 2026.
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Allogene Q4 net loss $38.8M; cash runway into Q1 2028; cema-cel ALPHA3 interim April 2026
Q4 net loss $38.8M ($0.17/share); FY 2025 net loss $190.9M ($0.87/share).
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Allogene Therapeutics Reports Q3 2025 Net Loss of $41.4M, Cash of $277.1M
Q3 2025 net loss $41.4M ($0.19 per share), cash $277.1M, cash runway into 2H 2027.
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Allogene reports patent infringement lawsuit against licensor Cellectis by Factor Bioscience
Factor Bioscience filed a complaint in Delaware against Cellectis and AstraZeneca on Sept 26, 2025, alleging TALEN gene-editing patent infringement.
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Allogene Q2 net loss $50.9M; highlights ALPHA3 trial progress and ALLO-329 autoimmune initiation
Net loss of $50.9M ($0.23/share) for Q2 2025; cash and investments $302.6M as of June 30, 2025.
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Allogene drops ALLO-647 after Grade 5 death; pivots to Dagger platform
Grade 5 hepatic failure from adenovirus attributed to ALLO-647; FC+ALLO-647 arm closed in ALPHA3 study.
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Allogene Q1 net loss $59.7M; ALPHA3 milestone delayed to 1H 2026; cash runway to 2H 2027
Net loss $59.7M ($0.28/sh); R&D $50.2M, G&A $15M; cash, equivalents & investments $335.5M.
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Allogene reports Q4 net loss $59.9M; cash $373.1M; pipeline milestones 2025-2027
Q4 net loss $59.9M ($0.28/share); FY net loss $257.6M ($1.32/share); R&D expense $45M Q4.
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Allogene discontinues enrollment in Phase 1 cema-cel CLL trial due to slow accrual
Discontinued the Phase 1 cohort in ALPHA2 trial for cema-cel in relapsed/refractory CLL after BTKi/BCL2i therapy.
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Allogene Q2 net loss $66.4M ($0.35/sh); initiated pivotal ALPHA3 trial for cema-cel
Net loss of $66.4M ($0.35 per share) includes $13.6M stock-based comp and $5.0M impairment.
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Allogene restructures JV; ownership diluted to 15.4%, license royalty amended to flat mid-single-digit
JV acquires Overland US (lead asset OL-101, autologous GPRC5D-BCMA CAR-T for multiple myeloma).
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Allogene Therapeutics raises $110M in registered equity offering at $2.90 per share with insider participation
Offering of 37,931,035 shares at $2.90 per share for gross proceeds of ~$110M; expected to close May 16, 2024.
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Allogene expands CD19 rights to EU/UK; Q1 net loss $65M; cash $397M into 2026
Expanded CD19 oncology rights to all EU Member States and UK from Servier; combined market opportunity increased to >$9.5B from $6B.
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Allogene reports Q4 net loss $85.8M, cash $448.7M; ALPHA3 trial to start mid-2024
Net loss Q4 2023 $85.8M ($0.51/share); full-year net loss $327.3M ($2.09/share).
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Allogene restates 2020-2022 financials; material weakness in ICFR identified
Audit Committee determined 2020-2022 annual and 2021-2023 quarterly reports should no longer be relied upon.
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Allogene amends Notch collaboration, retains exclusive rights to one CAR target, gives up others
Relinquished exclusive rights to all original CAR targets except one; option limited to one additional target.
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Allogene to start pivotal ALPHA3 trial in 1L LBCL; cuts 22% staff, partners with Foresight
Workforce reduction of ~22% with estimated $5.0M-$5.5M in severance charges, mostly in Q1 2024.
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Allogene gets FDA Fast Track for ALLO-647; safety data from 87 patients at ASH
FDA granted Fast Track Designation for ALLO-647 in adult patients with r/r LBCL.
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Allogene reports Q3 net loss $61.3M; cash $497.7M; ALPHA2 on track
Net loss of $61.3M ($0.37/sh) for Q3 2023; R&D expense $46.0M, G&A $17.0M.
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Allogene reports Q2 2023 net loss of $78.0M; cash extends into 2H 2025
Cash, equivalents, and investments $544.5M as of June 30, 2023; raised $87.9M via ATM in Q2.
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Allogene reports updated Phase 1 data for ALLO-501/501A in r/r LBCL with 58% ORR and 42% CR
In 33 CAR T-naïve patients, ORR 58%, CR 42%; 30% maintained CR at 6 months across all patients.
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Allogene reports 67% ORR and 58% CR in Phase 1 ALPHA/ALPHA2 trials of ALLO-501/501A in r/r LBCL
67% ORR and 58% CR in CAR T-naive r/r LBCL patients (n=12) treated with Phase 2 regimen at ASCO.
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Allogene reports Q1 net loss $98.7M, cash $514M; clinical progress in ALLO-501A and ALLO-316
Net loss $98.7M ($0.68/share); R&D $80.2M, G&A $18.9M; cash $514M as of March 31, 2023.
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Allogene Therapeutics has no cash deposits or securities at Silicon Valley Bank
Company confirms zero exposure to SVB amid its closure and industry uncertainty.
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Allogene reports Q4 2022 net loss $94.8M, cash $576.5M; pipeline advances
Net loss Q4 2022 $94.8M ($0.66/share); full year net loss $332.6M ($2.32/share).
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Allogene Therapeutics EVP of R&D Rafael Amado resigns effective Dec 30, 2022
Rafael G. Amado, Executive Vice President of Research and Development, resigned.
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Allogene releases Phase 1 data across CAR T programs; initiates Phase 2 ALPHA2 trial
Single Dose FCA90 in LBCL achieved 67% ORR, 58% CR; 50% in CR at 6 and 12 months. No Grade 3+ CRS or neurotoxicity.
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Allogene reports Q3 net loss of $83.1M; initiates first allogeneic CAR T Phase 2 trial
Net loss $83.1M ($0.58/share); R&D expenses $63.6M; G&A $18.9M.
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Allogene initiates Phase 2 ALPHA2 trial of ALLO-501A in r/r LBCL; plans EXPAND trial for ALLO-647
ALPHA2 trial will enroll ~100 r/r LBCL patients with single 120M CAR+ cell dose; primary endpoint ORR.
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Servier discontinues CD19 development; Allogene may exercise ex-US license at added cost
Servier sent discontinuation notice for CD19 products (UCART19, ALLO-501, ALLO-501A) per Servier Agreement.
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Allogene expects FDA clearance for first allogeneic CAR T pivotal trial; Q2 net loss $74.8M
FDA clearance expected in coming weeks for Phase 2 pivotal trial of ALLO-501A in LBCL; would be first allogeneic CAR T pivotal trial.
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Allogene reports Q1 net loss $79.9M, cash $733M; plans pivotal ALLO-501A trial mid-2022
Net loss $79.9M ($0.56/sh); R&D $60.2M, G&A $19.9M; cash $733.1M at March 31, 2022.