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Compass Therapeutics Q2 net loss $25.2M; tovecimig ORR improves to 18.0% with p=0.0228
Net loss of $25.2M ($0.13/sh) vs $19.9M ($0.14/sh) in Q2 2025; R&D spend rose 19% to $19.6M.
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Compass Therapeutics reports tovecimig Phase 2/3 COMPANION-002 met primary endpoint; BLA filing planned
Tovecimig + paclitaxel achieved ORR 18.0% vs 5.3% paclitaxel alone (p=0.0228); median PFS 4.7 vs 2.6 months (HR=0.44, p<0.0001).
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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: 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 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 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.
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Compass Therapeutics appoints Bisker-Leib as CEO, Schuetz to President of R&D
Vered Bisker-Leib appointed CEO effective Jan 9, 2024; salary increased to $600k, target bonus 55%.
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Compass Therapeutics: CEO change to Bisker-Leib, CTX-471 CR in SCLC, $152M cash
CEO succession: Vered Bisker-Leib appointed CEO effective Jan 9, 2024; Thomas Schuetz becomes President of R&D and Vice Chair.
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Compass Q3 net loss $10.0M ($0.08/shr); cash $164M; CEO succession to Bisker-Leib
Net loss for Q3 2023 was $10.0M ($0.08/shr) vs $12.0M ($0.12/shr) in Q3 2022; 9-month net loss $29.1M.
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Compass Therapeutics Q2 net loss $11.3M; BTC top-line data pushed to H2 2024
Net loss of $11.3M ($0.09/share) in Q2 2023 vs $8.5M loss ($0.08/share) in Q2 2022.
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Compass Therapeutics Q1 net loss $7.8M; cash $175M funds operations into 2026
Net loss of $7.8M ($0.06 per share) vs $7.2M in Q1 2022; R&D spend up 50% to $6.6M on CTX-009.
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Compass Therapeutics confirms no cash deposits or securities at Silicon Valley Bank
Company explicitly states it holds no cash deposits at Silicon Valley Bank.
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Compass Therapeutics reports positive Phase 2 data for CTX-009 in biliary tract cancers; ORR 37.5%
CTX-009 + paclitaxel achieved 37.5% ORR in 24 patients; second-line sub-group ORR 63.6% (7/11 PRs).
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Compass Therapeutics raises $80M in PIPE led by Enavate; extends cash runway to 2026
Issues 25M shares at $3.21 each for gross proceeds of ~$80M; closing expected by Nov 8, 2022.
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Compass reports CTX-009 42% ORR in biliary tract cancers; to start U.S. Phase 2 in Q3 2022
CTX-009 + paclitaxel achieved 42% ORR (10 PRs) out of 24 patients with advanced biliary tract cancers.
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FDA clears IND for Compass Therapeutics' CTX-009 Phase 2 study in biliary tract cancers
FDA cleared IND for CTX-009 bispecific antibody targeting DLL4 and VEGF-A.
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Compass Therapeutics prices $125M public offering of 35.7M shares at $3.50; uplists to Nasdaq
Underwritten public offering of 35,715,000 shares at $3.50/share; underwriters have 30-day option for additional 5,357,250 shares.
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Compass reports CTX-009 Phase 2a ORR 29% in BTC; proposes public offering and Nasdaq uplist
CTX-009 Phase 2a in biliary tract cancer met criteria to advance; 5 partial responses in 17 patients (ORR 29%), 100% clinical benefit rate.
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Compass Therapeutics reports CTX-009 Phase 1 data: 19% ORR at RP2D in heavily pre-treated tumors
CTX-009 monotherapy achieved 19% ORR (3/16) at RP2D (10.0-12.5 mg/kg) and 69% DCR.
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Compass Therapeutics merger with Trigr completed; Trigr had $99k cash, $15.8M deficit
Trigr audited 2020: cash $99k, total liabilities $2.57M, net loss $2.11M, accumulated deficit $15.8M; going concern doubt.