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Compass Therapeutics reports tovecimig Phase 2/3 BTC data with significant PFS benefit; BLA planned
Tovecimig + paclitaxel: ORR 17.1% vs 5.3% (p=0.031); PFS 4.7 vs 2.6 months (HR=0.44, p<0.0001); OS crossover benefit.
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Compass reports tovecimig hits PFS endpoint in BTC Ph2/3; plans BLA submission
Tovecimig + paclitaxel met key secondary PFS endpoint: median 4.7 vs 2.6 months (HR=0.44, p<0.0001).
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Compass Therapeutics reports 2025 net loss of $66.5M; tovecimig PFS/OS data due in April
Net loss $66.5M ($0.42/share) vs $49.4M ($0.36/share) in 2024; R&D spend up 32% to $56.0M.
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Compass Therapeutics reports $209M cash, tovecimig PFS/OS data on track Q1 2026; appoints CCO and CMO
Cash and marketable securities estimated at $209M as of Dec 31, 2025; cash runway into 2028.
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Compass Therapeutics Q3 2025 net loss $14.3M; cash $220M; tovecimig OS/PFS data late Q1 2026
Net loss Q3 2025 $14.3M ($0.08/share) vs $10.5M ($0.08) Q3 2024; nine-month loss $50.8M ($0.34).
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Compass Therapeutics prices $120M upsized public offering of common stock and pre-funded warrants
Priced upsized $120M offering: 33.29M shares at $3.00/share and 6.71M pre-funded warrants at $2.9999 each.
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Compass Q2 net loss $19.9M; CTX-8371 shows deep responses; tovecimig OS readout moves to Q1 2026
Net loss Q2 2025 $19.9M ($0.14/share) vs $13.1M ($0.10/share) in Q2 2024; R&D expenses rose 47% to $16.4M.
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Compass Therapeutics annual meeting elects three directors, ratifies auditor
Carl L. Gordon, Philip J. Ferneau, and James P. Boylan elected as Class II directors with 80.7M, 58.3M, and 83.6M votes for, respectively.
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Compass Therapeutics: Tovecimig meets primary endpoint in BTC trial; Q1 net loss $16.6M
Tovecimig + paclitaxel achieved 17.1% ORR (incl. 1 complete response) vs 5.3% for paclitaxel alone (p=0.031) in Phase 2/3 BTC study.
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Tovecimig meets primary endpoint in Phase 2/3 BTC trial: 17.1% ORR vs 5.3% (p=0.031)
ORR 17.1% for tovecimig+paclitaxel (19/111) vs 5.3% for paclitaxel alone (3/57), p=0.031, statistically significant.
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Compass Therapeutics reports FY2024 net loss of $49.4M; tovecimig data expected end Q1 2025
Net loss $49.4M ($0.36/shr) vs $42.5M ($0.33) in 2023; R&D expense $42.3M (+11%).
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Compass Therapeutics provides pipeline update; cash at $127M, tovecimig data Q1 2025
Estimated $127M cash at YE 2024; cash runway expected into Q1 2027.
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Compass Therapeutics appoints Barry Shin as CFO; Neil Lerner as PAO
Barry Shin named CFO effective Dec 9, 2024; base salary $475K, target bonus 45%, sign-on $50K, and equity grants of 800K shares total.
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Compass Therapeutics Q3 2024 net loss $10.5M ($0.08/share); cash $135M
Net loss $10.5M vs $10.0M in Q3 2023; diluted EPS $0.08 unchanged.
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Compass Therapeutics Q2 net loss $13.1M; CTX-009 BTC trial enrollment completed, top-line data Q1 2025
Net loss of $13.1M ($0.10 per share) for Q2 2024 vs $11.3M loss in Q2 2023.
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Compass Therapeutics shareholders elect Chiniara and Gray, ratify auditor
Ellen V. Chiniara received 76,766,213 for and 23,754,485 withheld as director.
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Compass Therapeutics CEO Vered Bisker-Leib resigns; Thomas Schuetz appointed CEO
Vered Bisker-Leib, PhD, MBA resigned as CEO and board member effective May 28, 2024, not due to any disagreement.
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Compass Therapeutics Q1 net loss $10.8M; cash $156.3M; FDA Fast Track for CTX-009
Net loss $10.8M ($0.08/share) vs $7.8M ($0.06) in Q1 2023; R&D expenses rose to $9.5M.
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FDA grants Fast Track Designation for Compass's CTX-009 in biliary tract cancer
FDA Fast Track Designation for CTX-009 (bispecific DLL4/VEGF-A antibody) + paclitaxel in previously treated metastatic/locally advanced biliary tract cancer.
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Compass Therapeutics reports FY2023 net loss of $42.5M; CTX-009 data expected by end 2024
Net loss $42.5M ($0.33/share) vs $39.2M loss in 2022; R&D expenses rose 27% to $38.1M.