Abstract 719TiP
Background
HRO761 is a first-in-class selective WRN inhibitor that binds allosterically to the helicase domain of the WRN protein locking it in an inactive conformation. HRO761 has shown anti-tumor activity in MSIhi preclinical models.
Trial design
This is a phase I/Ib (NCT05838768), global, multicenter (approximately 27 sites to open across 14 countries) dose finding study that consists of a dose escalation part to allow the determination of a dose range for optimization (DRO) or a recommended dose (RD) for HRO761 single agent (s.a.), and an optional randomized dose optimization part (Arm A). HRO761 will be administered orally daily in a 28-day cycle. The dose escalation part will enroll MSIhi/dMMR advanced/metastatic (a/m) CRC and solid tumors (approximately 40 patients), and the randomized dose optimization part will enroll patients with a/m MSIhi /dMMR CRC (20 patients per dose) and solid tumors (up to 10 pts per dose). Based on an integrated analysis of the safety, tolerability, pharmacokinetic, pharmacodynamic, and preliminary anti-tumor activity data of HRO761, RD will be determined and subsequently tested in optional expansion arms of a/m MSIhi/dMMR CRC (20-40 patients), and solid tumor (20-40 patients). HRO761 at the RD will be investigated in a dose escalation in combination with either tislelizumab (Arm B) or irinotecan (Arm C) to determine the RD of the combinations. After the determination of the RDs, the combination treatments will be tested in expansion cohorts of a/m MSIhi or dMMR CRC and other solid tumors. AEs will be assessed according to CTCAE v5. Tumor response will be determined according to RECIST 1.1 criteria. Key eligibility criteria include: 1) Patients with advanced unresectable or metastatic MSIhi or dMMR solid tumors who have progressed after or are intolerant to prior standard therapy; 2) patients should have received at least one prior line of chemotherapy or targeted therapy, and prior immune checkpoint inhibitor therapy (Arm A and C). Checkpoint inhibitor therapy is permitted but not required and prior adjuvant therapy is allowed in Arm B.
Clinical trial identification
NCT05838768, First posted 3 May 2023.
Editorial acknowledgement
None to declare
Legal entity responsible for the study
Novartis Pharmaceuticals.
Funding
Novartis Pharmaceuticals.
Disclosure
M. Moschetta, H. Möbitz, I. Jaco, M. Cortes Cros, S. Ferretti, D. Jankovic, M. Thérier, G. Clementi, Y. Li, R. De Kanter, C. Quadt: Financial Interests, Personal, Stocks/Shares: Novartis; Financial Interests, Personal, Full or part-time Employment: Novartis. T. Doi: Financial Interests, Institutional, Research Grant: Taiho, MSD, AbbVie, Eisai, Pfizer, BMS, Janssen Pharma, Daiichi Sankyo, Chugai Pharma, Boehringer Ingelheim, PRA Health Sciences, Amgen, GSK, SHIONOGI, RIN Institute, ONO Pharma; Financial Interests, Personal, Advisory Role: Noile-Immune Biotech, Oncolys BioPharma, Boehringer Ingelheim, A2 Healthcare, Nano Carrier, PRA Health Sciences, KAKEN Pharma, Chugai Pharma, Sumitomo Pharma, Shionogi, Otsuka Pharma, Takeda, Kyowa Kirin, Rakuten Medical, Gilead; Financial Interests, Personal, Invited Speaker: Daiichi Sankyo. Y. Kuboki: Financial Interests, Institutional, Research Grant: Taiho, Astellas, Eli Lilly, Takeda, Daiichi Sankyo, AstraZeneca, Boehringer Ingelheim, Chugai, Genmab, Incyte, AbbVie, Amgen, Merk ; Financial Interests, Personal, Advisory Role: Incyte, Takeda, Boehringer Ingelheim, Amgen; Financial Interests, Personal, Speaker, Consultant, Advisor: Taiho, Eli Lilly, Takeda. R. Sundar: Financial Interests, Personal, Advisory Board: Bristol Myers Squibb, Merck, Eisai, Bayer, Taiho, Novartis, MSD, GSK, DKSH, Astellas; Financial Interests, Personal, Invited Speaker: MSD, Eli Lilly, BMS, Roche, Taiho, AstraZeneca, DKSH, Ipsen; Financial Interests, Personal, Stocks/Shares: Teladoc; Financial Interests, Institutional, Advisory Board: Paxman Coolers; Financial Interests, Personal and Institutional, Local PI: Taiho, MSD, BMS, Novartis; Non-Financial Interests, Advisory Role: Paxman Coolers; Non-Financial Interests, Principal Investigator: MSD, Natera.
Resources from the same session
668P - Efficacy and safety of larotrectinib in a pooled analysis of patients (Pts) with tropomyosin receptor kinase (TRK) fusion cancer
Presenter: Alexander Drilon
Session: Poster session 17
669P - Patient-reported outcomes with selpercatinib in patients with RET-driven cancers in the phase I/II LIBRETTO-001 trial
Presenter: Hyunseok Kang
Session: Poster session 17
670P - Preliminary efficacy and safety of tinengotinib (TT-00420) monotherapy in Chinese patients (pts) with advanced solid tumors: Results from a phase Ib/II study
Presenter: Panpan Zhang
Session: Poster session 17
671P - Safety and efficacy of PM060184 plus gemcitabine in advanced solid tumors
Presenter: Sanjay Goel
Session: Poster session 17
672P - Phase I/II trial of RVU120 (SEL120), CDK8/CDK19 inhibitor in patients with relapsed/refractory metastatic or advanced solid tumors
Presenter: Rafal Dziadziuszko
Session: Poster session 17
673P - A phase I dose-escalation and expansion study evaluating the safety and efficacy of the MDM2–p53 antagonist brigimadlin (BI 907828) in patients (pts) with solid tumours
Presenter: Patrick Schoeffski
Session: Poster session 17
674P - Response of thrombopoietin receptor agonists in MDM2 inhibitor induced thrombocytopenia
Presenter: Raymond DeMatteo
Session: Poster session 17
675P - A phase I study of safety, pharmacokinetics, and pharmacodynamics of SCR-6920, a protein arginine methyltransferase 5 (PRMT5) inhibitor, in patients with advanced malignant tumors
Presenter: Jinming Yu
Session: Poster session 17
676P - Preclinical characterization of novel peptide binders for EphA2-targeted radiopharmaceutical therapy
Presenter: Renee Clift
Session: Poster session 17
677P - Preliminary findings from a phase I, open-label, dose-finding study of SNB-101 in patients with advanced solid tumors
Presenter: Yun Beom Sang
Session: Poster session 17