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Caribou Q2 2026 net loss $24.3M; vispa-cel and CB-011 show strong efficacy data
Q2 2026 net loss $24.3M ($0.24/share) vs $54.1M ($0.58) in Q2 2025, which included $21.3M impairment.
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Caribou Biosciences shareholders reject officer exculpation amendment at annual meeting
Proposal 3 (officer exculpation) failed: 37.5M for, 3.5M against, 27.1M broker non-votes.
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Caribou reports vispa-cel 82% ORR, 17.1mo mPFS in 2L LBCL; CB-011 83% CR rate in MM
Vispa-cel in 27 optimized 2L LBCL patients: 82% ORR, 67% CR, 17.1 months median PFS.
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Caribou Q1 2026 rev flat at $2.4M; FDA aligns on pivotal trial for vispa-cel
FDA alignment on ANTLER-3 pivotal phase 3 trial for vispa-cel in 2L LBCL; primary endpoint PFS, crossover allowed.
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Caribou gets RMAT designation from FDA for CB-011 in relapsed/refractory multiple myeloma
FDA grants Regenerative Medicine Advanced Therapy (RMAT) designation for CB-011 allogeneic anti-BCMA CAR-T.
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Caribou Biosciences FY2025 net loss $148.1M; cash $142.8M funds into 2H 2027
GAAP net loss FY2025 $148.1M ($1.59/sh) vs $149.1M ($1.65) prior year; non-GAAP loss $126.8M excluding $21.3M impairment.
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Caribou Biosciences reports Q3 2025 clinical data: vispa-cel 86% ORR, CB-011 92% ORR; cash $159.2M
Vispa-cel ANTLER phase 1: 86% ORR, 63% CR, 53% PFS at 12mo in 35 patients with optimized profile (≥2 HLA match, young donor).
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Caribou reports positive vispa-cel phase 1 data: 82% ORR, 64% CR in 2L LBCL; cash ~$159.2M
Vispa-cel confirmatory cohort (N=22): 82% ORR, 64% CR rate, 51% 12-month PFS in 2L LBCL.
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Caribou Q2 net loss $54.1M ($0.58/sh); clinical data on track for H2 2025
GAAP net loss $54.1M ($0.58/sh) vs $37.7M ($0.42/sh) in Q2 2024; non-GAAP loss $32.8M ($0.35/sh) excluding $21.3M impairment.
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Caribou Biosciences regains Nasdaq minimum bid price compliance after 10-day period above $1.00
Received Nasdaq compliance notice on June 18, 2025, confirming regained compliance with Listing Rule 5450(a)(1).
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Caribou Biosciences stockholders approve reverse stock split authorization at annual meeting
Class I directors elected: Scott Braunstein (40.2M votes for) and Ran Zheng (30.4M votes for).
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Caribou Q1 net loss $40M; cuts 32% workforce, extends cash runway into H2 2027
Cash, equivalents & securities $212.5M as of Mar 31, 2025 (down from $249.4M at Dec 31, 2024).
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Caribou cuts 32% workforce, discontinues lupus/AML trials, cash runway to H2 2027
Workforce reduction of 47 employees (~32%), expected completion by Q2 2025.
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Caribou Biosciences Q4/FY2024 net loss $149.1M; cash $249.4M into H2 2026; CSO retiring
Net loss $149.1M in 2024 vs $102.1M in 2023; revenue fell to $10.0M from $34.5M on AbbVie deal end.
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Caribou Biosciences initiates lupus trial, plans 2025 data milestones, hires new CFO
Initiated GALLOP Phase 1 trial of CB-010 in lupus nephritis and extrarenal lupus; FDA Fast Track for refractory SLE.
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Caribou Biosciences appoints Sri Ryali as CFO, effective January 2, 2025
Sri Ryali named CFO; brings 20 years biopharma finance experience; most recently CFO of Codexis.
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Caribou Q3 net loss $34.7M vs $10.0M YoY; cash $281M funds into H2 2026
Revenue $2.0M, down from $23.7M due to AbbVie termination; R&D expense $30.4M.
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Caribou Biosciences appoints Ryan Fischesser interim CFO and grants 25,000 RSUs
Ryan Fischesser designated interim principal financial officer and accounting officer effective Sept 27, 2024, following Jason O'Byrne's resignation.
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CFO Jason O'Byrne resigns effective Sept 27; Ryan Fischesser named principal accounting officer
Jason O'Byrne resigns as CFO effective Sept 27, 2024, to pursue other opportunity; no disagreement with company.
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Caribou Biosciences appoints Tina Albertson, MD PhD, as Chief Medical Officer
Dr. Albertson brings 15 years of experience in cellular therapy development, most recently as CMO at Lyell Immunopharma.
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Caribou Q2 net loss $37.7M; extends cash runway to H2 2026 after 12% workforce cut
Net loss $37.7M in Q2 2024 vs $29.5M in Q2 2023; cash & equivalents $311.8M at June 30, down from $372.4M.
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Caribou discontinues CAR-NK platform, cuts 12% workforce to extend cash runway into H2 2026
Preliminary cash $311.8M at June 30, 2024; expects to report Q2 results later.
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Caribou Biosciences stockholders elect three directors and ratify auditor at 2024 annual meeting
Elected Class III directors: Rachel Haurwitz (57.4M for), Dara Richardson-Heron (50.2M for), Natalie Sacks (50.2M for).
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Caribou Biosciences reports CB-010 ANTLER Phase 1 data: 14.4 mo median PFS with partial HLA matching
Median PFS of 14.4 months with ≥4 HLA matches (N=13) vs 2.8 months with ≤3 matches (N=33).
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Caribou Q1 net loss $41.2M; cash $345.9M; IND cleared for CB-010 in lupus
Net loss of $41.2M for Q1 2024 vs $28.0M in Q1 2023; R&D expenses rose to $33.8M.
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Caribou Biosciences receives FDA IND clearance for CB-010 in lupus; GALLOP Ph1 trial expected by YE 2024
FDA cleared IND for CB-010 (allogeneic anti-CD19 CAR-T) to treat lupus nephritis and extrarenal lupus.
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Caribou Biosciences reports FY 2023 net loss $102.1M, cash $372.4M; clinical updates
Net loss $102.1M in FY 2023 vs $99.4M in FY 2022; R&D expenses rose to $112.1M.
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Caribou appoints Tim Kelly as CTO; plans CB-010 pivotal trial by YE 2024, cash into Q4 2025
Tim Kelly appointed CTO; previously CEO of Oxford Biomedica Solutions, led technical ops at Sarepta, Shire, and Biogen.
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Caribou Biosciences CMO Syed Rizvi to leave Dec 31, 2023; severance terms set
Dr. Rizvi's departure effective Dec 31, 2023; previously announced Dec 12, 2023.
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Caribou reaches FDA alignment on CB-010 phase 3 trial design; CMO to depart Dec 31
FDA accepts comparator arm of platinum-based immunochemotherapy + HDCT + ASCT for CB-010 phase 3 in 2L r/r LBCL.
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Caribou Biosciences Q3 net loss $10M, cash $396.7M; pipeline advances with CB-010, CB-011, CB-012
Net loss of $10.0M for Q3 2023 vs $26.6M in Q3 2022; revenue $23.7M (incl. $21.5M from AbbVie termination).
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Caribou Biosciences gets FDA IND clearance for CB-012 allogeneic CAR-T in r/r AML
FDA cleared IND for CB-012, an allogeneic anti-CLL-1 CAR-T cell therapy for relapsed/refractory AML.
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AbbVie terminates collaboration with Caribou for two allogeneic CAR-T programs; effective Oct 25, 2023
AbbVie exercised termination for convenience, citing strategic focus; not related to Caribou's performance or data.
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Caribou Q2 net loss $29.5M; CB-010 shows 94% ORR; cash runway into Q4 2025
Net loss of $29.5M for Q2 2023 versus $26.7M in Q2 2022; R&D expenses $26.5M.
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Caribou Biosciences prices upsized $125M public offering at $6.50/sh
Priced 19,230,769 shares at $6.50 per share; underwriters granted 30-day option for 2,884,615 additional shares.
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Caribou announces positive long-term follow-up from ANTLER Phase 1 of CB-010
Positive long-term follow-up results from dose escalation portion of ANTLER Phase 1 trial.
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Caribou announces positive long-term follow-up for CB-010 in ANTLER Phase 1
Positive long-term follow-up results from dose escalation of ANTLER Phase 1 for CB-010 in relapsed/refractory B-NHL.
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CB-010 Phase 1 data: 94% ORR, 69% CR in r/r B-NHL; 44% CR ≥6 months; cash ~$292.5M
CB-010 achieved 94% ORR (15/16) and 69% CR (11/16) in r/r B-NHL patients in ANTLER Phase 1 dose escalation.
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Pfizer invests $25M in Caribou at $5.33/sh; gains SAB seat & BCMA first negotiation rights
Pfizer purchased 4,690,431 shares at $5.33/sh for ~$25M; deal closed June 30, 2023.
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Caribou stockholders elect Guggenhime, Johnson, Whiting as Class II directors and ratify Deloitte as auditor
Andrew Guggenhime: 31.0M votes for, 5.3M withheld, 9.4M broker non-votes.
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Caribou Q1 net loss $28M, cash $291M; CB-010 dose expansion enrolling, CB-011 dosing initiated
Net loss of $28.0M in Q1 2023, vs $19.1M in Q1 2022, driven by higher R&D expenses.
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Caribou Biosciences gets FDA Fast Track for CB-011 CAR-T in relapsed/refractory multiple myeloma
CB-011 is an allogeneic anti-BCMA CAR-T with immune cloaking (B2M-HLA-E transgene).
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Caribou initiates dose expansion of CB-010 ANTLER trial in second-line LBCL patients
CB-010 is first allogeneic CAR-T evaluated in second-line LBCL, per company.
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Caribou Biosciences doses first patient in Phase 1 trial of CB-011 for multiple myeloma
First patient dosed with CB-011 at dose level 1 (50x10^6 CAR-T cells) in CaMMouflage Phase 1 trial for relapsed/refractory multiple myeloma.
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Caribou Biosciences schedules 2023 annual meeting for June 15, 2023
Annual meeting will be held virtually on June 15, 2023 at 7:30 a.m. PDT.
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Caribou Q4 net loss $27M; cash $317M; CB-010 data update planned H2 2023
Net loss of $27.0M in Q4 2022 and $99.4M for full year 2022, vs. $18.5M and $66.9M in 2021.
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Caribou appoints CFO Jason O'Byrne as principal accounting officer; controller Fischesser cedes role
Jason V. O'Byrne, CFO, appointed principal accounting officer effective Dec 15, 2022.
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Caribou: 12-month CB-010 data shows durable CR in 2/6; selects ROR1 for CB-020
CB-010 ANTLER cohort 1: 6/6 CR best response; 3/6 durable CR at 6 months; 2/6 maintain CR at 12 months; longest CR 18 months.
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Caribou Bio receives RMAT and Fast Track designations from FDA for CB-010 CAR-T therapy
FDA grants RMAT for relapsed/refractory large B cell lymphoma (LBCL) and Fast Track for r/r B-NHL for CB-010.
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Caribou Biosciences receives FDA IND clearance for CB-011, allogeneic anti-BCMA CAR-T therapy for multiple myeloma
CB-011 is a genome-edited allogeneic anti-BCMA CAR-T cell therapy with immune cloaking.