3013 Background: B7-H4, a transmembrane glycoprotein, has limited expression in normal tissue, but is upregulated in a variety of solid tumors. BG-C9074 is an investigational topoisomerase I inhibitor antibody-drug conjugate (ADC) that targets B7-H4. We present results of monotherapy dose escalation and safety expansion from the ongoing phase 1 study. Methods: BG-C9074-101 (NCT06233942) is a first-in-human, multicenter study of BG-C9074 as monotherapy and in combination with other anticancer therapies in patients (pts) with advanced solid tumors. Pts with advanced solid tumors, irrespective of B7-H4 expression, received BG-C9074 IV every 3 weeks in escalating doses from 1 to 9 mg/kg. Endpoints included safety, preliminary antitumor activity (per RECIST v1.1) and pharmacokinetics. Results: As of Dec 29, 2025, 123 pts with advanced solid tumors received BG-C9074 monotherapy in phase 1a (ovarian OC, n = 62; HR+/HER2- breast cancer, n = 28; triple negative breast cancer TNBC, n = 18; cholangiocarcinoma, n = 11; endometrial, n = 3; squamous non-small cell lung cancer, n = 1). Median (range) prior lines were 4 (0-13). 8 pts experienced DLTs (thrombocytopenia n = 2, 6.5 mg/kg; n = 1, 7 mg/kg, febrile neutropenia n = 1, 6.5 mg/kg; n = 1, 7 mg/kg, neutropenic infection n = 1, 7 mg/kg, fatigue n = 1, 6 mg/kg, nausea n = 1, 9 mg/kg, and unexplained death n = 1, 9 mg/kg). Treatment-related adverse events (TRAEs) occurred in 113 pts (91.9%); grade (gr) ≥3 in 30.1%. The most common TRAEs were nausea (53.7%; gr ≥3, 4.1%), neutrophil count decreased/neutropenia (44.7%; gr ≥3, 18.7%), and fatigue (37.4%; gr ≥3, 2.4%). Hematologic and gastrointestinal toxicities were manageable with dose modifications and/or supportive care. Among 114 efficacy-evaluable pts, confirmed ORR (cORR) was 28.1% (95% CI: 20.1-37.3), including 2 CRs (1 OC, 6.5 mg/kg, 1 TNBC, 5 mg/kg) and 30 PRs (Table); unconfirmed ORR was 33.3% (24.8-42.8; 3 CRs, 35 PRs). Responses were observed across doses and levels of B7-H4 expression, without consistent association of response with B7-H4 expression across tumor types. Median (range) study follow-up was 6.0 (0.3-17.7) months. ADC and free payload concentrations decreased in a biexponential manner with a half-life of ~7 days for ADC. Exposure for ADC and free payload increased approximately dose proportionally. Conclusions: BG-C9074 demonstrates a tolerable safety profile in pts with advanced solid tumors. Encouraging antitumor activity was observed in OC and TNBC. Dose expansion and optimization are ongoing. Clinical trial information: NCT06233942 . OC (n=55) TNBC (n=16) HR+/HER2- BC (n=28) Total (N=114) cORR, % (95% CI) 34.5(22.2-48.6) 31.3(11.0-58.7) 17.9(6.1-36.9) 28.1(20.1-37.3) CR, n (%) 1 (1.8) 1 (6.3) 0 (0.0) 2 (1.8) PR, n (%) 18 (32.7) 4 (25.0) 5 (17.9) 30 (26.3) SD, n (%) 32 (58.2) 5 (31.3) 16 (57.1) 60 (52.6) PD, n (%) 4 (7.3) 5 (31.3) 7 (25.0) 17 (14.9) Not evaluable, n (%) 0 (0.0) 1 (6.3) 0 (0.0) 5 (4.4)
Xu et al. (Wed,) studied this question.