A phase 1, first-in-human (FIH) study evaluating the safety, pharmacokinetics, and efficacy of ABBV-969 in patients with metastatic castration-resistant prostate cancer (mCRPC).

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Authors: Tanya B. Dorff, Avivit Peer, Manish R. Sharma, Anthony M. Joshua, John D. Powderly, Yutaka Shimazu, Rahul Raj Aggarwal, Benedito A. Carneiro, Russell Zelig Szmulewitz, Linu Abraham, Sumiko Okubo, Claudina Stevenson
+8 more Samaneh Alaei, Song Wang, Muhammad Jalaluddin, Oluwadamilola Ogunyankin, Sarah Mudd, David I. Quinn, Fred Saad, Anthony W. Tolcher
Cited by: 2

Abstract

5014 Background: Prostate-specific membrane antigen (PSMA) and six-transmembrane epithelial antigen of prostate 1 (STEAP1) are overexpressed in >80% of metastatic prostate cancer tumors. ABBV-969 is a first-in-class PSMA/STEAP1 dual-targeting antibody drug conjugate with a topoisomerase 1 inhibitor (Top1i) payload. We report results from the completed dose escalation part of the phase 1, FIH study (NCT06318273) evaluating ABBV-969 in patients (pts) with mCRPC. Methods: Pts were ≥18 years with confirmed metastatic prostate adenocarcinoma, had an ECOG performance score ≤1, a serum prostate-specific antigen (PSA) level ≥1.0 ng/mL, and hemoglobin ≥9 g/dL at study entry. Pts received ≥1 novel hormone agent (NHA) and ≥1 taxane (unless unable to receive or declined taxane), and progressed on prior NHA. Pts received 1 mg/kg–12.5 mg/kg of ABBV-969 monotherapy every 3 weeks until disease progression or intolerable toxicity. Primary objective was to determine safety and tolerability. Secondary objectives were preliminary efficacy, pharmacokinetics, and recommended phase 2 dose. Results: As of Jan 2026, 49 pts with mCRPC received ABBV-969 in the dose escalation part of the study. Median follow-up was 11.1 months (95% CI, 8.4–13.2), and median number of prior lines was 5 (range 1–9). Pt demographics and safety results are shown in Table 1. Thirty-one (63%) pts had Grade (G) ≥3 TEAEs, primarily G3 anemia (n=24). Dose and exposure responses were observed, with durable PSA and objective responses noted at all dose levels ≥3 mg/kg. At dose levels ≥3 mg/kg, confirmed PSA50 and PSA90 responses were 67% (95% CI, 52–81) and 28% (95% CI, 15–44), respectively. Among 29 pts with RECIST-evaluable disease, the confirmed ORR, as assessed by investigator, was 45% (95% CI, 26–64). At data cut, 26 pts were receiving ongoing treatment. Radiographic PFS will be presented. Conclusions: ABBV-969 demonstrated promising antitumor activity and a manageable safety profile in heavily pretreated pts with mCRPC. Dose optimization is ongoing. Clinical trial information: NCT06318273 . Pt demographics and safety. TotalN=49 Median age, years (range) 71 (57–84) Median PSA, µg/L (range) 74 (2–2879) Disease location, n (%)BoneLymph nodeLiverLungAdrenal gland 43 (88)20 (41)8 (16)7 (14)2 (4) Prior therapy, n (%) a Androgen-receptor pathway inhibitorDocetaxelCabazitaxel 177 Lu-PSMA-617 49 (100)41 (84)19 (39)23 (47) Any Grade TEAE of interest, n (%)Hematologic toxicityGastrointestinal toxicitySalivary gland toxicity 38 (78)33 (67)6 (12) TEAE leading to, n (%)Discontinuation b InterruptionReduction 3 (6)24 (49)16 (33) TEAE leading to death, n (%) c Pneumonitis c 1 (2)1 (2) DLT events, n (%) d 3 (6) a Only therapies of interest listed. b G3 pneumonitis and disease progression. c ABBV-969-related. d Anemia at ≥8 mg/kg doses. DLT, dose-limiting toxicity.

Fields of Study & Subjects

Prostate Cancer Treatment and Research HER2/EGFR in Cancer Research PARP inhibition in cancer therapy

Publication details

Journal / source
Journal of Clinical Oncology
Publisher
American Society of Clinical Oncology (ASCO)
Volume
44
Issue
16_suppl
Pages
5014–5014
Publication date
27 May 2026
Language
EN