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
107P - Comprehensive genomic profiling of “The German-registry of incidental gallbladder carcinoma” cases
Presenter: Nihat Bugra Agaoglu
Session: Poster session 17
108P - FGFR2 fusions and their impact on efficacy of standard chemotherapy in patients with biliary tract cancer
Presenter: Binbin Zheng-Lin
Session: Poster session 17
109P - DNA damage repair pathways in biliary tract cancer: A new target for precision medicine?
Presenter: Ilektra Mavroeidi
Session: Poster session 17
110P - Detection of HER2 overexpression in biliary tract cancers: Comparison of AmoyDx® HER-2 (29D8) assay with ventana PATHWAY anti-HER-2/neu (4B5) assay
Presenter: Hui Dong
Session: Poster session 17
111P - The concordance between circulating tumor DNA and tissue genomic profiling in patients with advanced biliary tract cancer
Presenter: Seonjeong Woo
Session: Poster session 17
112P - Clinical, genomic and transcriptomic characteristics of young-onset biliary tract cancers
Presenter: Thomas Pudlarz
Session: Poster session 17
113P - Molecular profiling of biliary tract cancers in patients of African and European ancestries
Presenter: Zishuo Hu
Session: Poster session 17
114P - Prospective longitudinal tumor-informed ctDNA in resectable biliary tract cancers
Presenter: Gentry King
Session: Poster session 17
115P - Inhibition of KLF5 reduces tumor growth and sensitizes to chemotherapy-induced cell death in experimental models of cholangiocarcinoma
Presenter: Ana Landa Magdalena
Session: Poster session 17