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Compass Therapeutics (CMPX) investor relations material
Compass Therapeutics Evercore ISI 8th Annual HealthCONx Conference summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Strategic pipeline updates and clinical milestones
Four oncology drugs in development, with three in the clinic and a fourth entering trials early next year.
Lead program Tevecimig (DLL4 VEGF-A bispecific) to report PFS and OS secondary endpoints in Q1 2026.
PD-1, PD-L1 bispecific antibody showed three responses in first 15 patients, including refractory cases; cohort expansions in TNBC and NSCLC planned.
Novel PD-1 VEGF-A bispecific entering clinic early next year, with four phase I indications planned.
CD137 agonist antibody to begin biomarker-driven basket study in first half of next year.
Clinical data highlights and efficacy signals
Tevecimig tripled response rate over control in BTC, with lower progressive disease incidence (16% vs 42% at week 8).
Fewer deaths than projected in randomized BTC study, suggesting improved OS and a potential tail on the Kaplan-Meier curve.
Median PFS in phase II BTC study was 9.4 months; conservative lower bound at 5.4 months, exceeding current second-line chemotherapy.
PD-1, PD-L1 bispecific showed responses in heavily pretreated, post-checkpoint patients, including near CR in NSCLC and durable response in TNBC.
No dose-limiting toxicities observed up to 10 mg/kg in phase I PD-1, PD-L1 bispecific study.
Market opportunity and commercial strategy
Second-line BTC market estimated at 15,000 US patients annually, with potential for six months on drug and multi-billion-dollar opportunity.
Frontline BTC expansion ongoing at MD Anderson, with potential to increase patient pool by 50%.
Additional expansion opportunities in DLL4-expressing tumors: hepatocellular, gastric, ovarian, renal cell, and colorectal cancers.
Commercial-ready manufacturing process established for Tevecimig; pre-launch and prescriber awareness initiatives underway.
Academic medical centers involved in trials position the company for strong prescriber engagement ahead of a potential 2027 launch.
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