Abstract 694P
Background
Clever-1 is an immunosuppressive scavenger receptor expressed on tumor associated macrophages. Bexmarilimab (FP-1305) is a novel humanized anti-CLEVER-1 IgG4-antibody capable of switching tumor macrophage phenotype leading to T-cell mediated anti-tumor responses.
Methods
MATINS (Macrophage Antibody To INhibit immune Suppression) trial is a first-in-human phase I/II study (NCT03733990) to assess safety and preliminary efficacy of Bexmarilimab (Bex) in patients with refractory advanced solid tumours. Part I has been completed with initial adequate safety profile, preliminary signs of efficacy, and initial recommended dose of 1mg/kg Q3W for part II. In Part II, 10 patients with distinct solid tumour types and variable doses and dosing frequency of Bex were studied to investigate safety, tolerability and efficacy.
Results
At the data cut-off of Apr 17th 2023, 214 patients have been enrolled to the study. In the alternative dosing cohorts, 66 patients were exposed to Bex with 1-3mg/kg Q1W, 1-3mg/kg Q2W, or 3-30mg/kg Q3W dosing. Bex was well tolerated with fatigue (15.9%) and pyrexia (5.6%) being the most frequent treatment related adverse event (TRAE) and 7.9% of the patients experiencing grade 3-4 TRAE. Disease control rate (DCR) was 13.0% (n=28) overall. Highest disease control rates (DCR) were observed in hepatocellular cancer (36%), ER+ breast cancer (33%), cutaneous melanoma (22%), and cholangiocarcinoma (21%). DCR was associated with Bex-induced immune activation in blood and tumor. Median progression-free survival was 2.0 and overall survival 5.6 months. 18-month survival rates (landmark analysis) were 32.9% in patients achieving DCR while this was 5.5% in non-DCR patients. The PFS ratio (defined by the PFS on bex/duration of previous treatment line) was > 1.3 in 46.4% of the DCR patients while this was 9.6% in non-DCR patients (p<0.0001). In the alternative dosing regimens, no dose-dependency was observed to adverse events or DCR rates.
Conclusions
Bexmarilimab demonstrates promising anti-tumour activity as a monotherapy in several refractory solid tumours. A dose of 1mg/kg Q3W is considered feasible for further monotherapy studies in solid tumors.
Clinical trial identification
NCT03733990.
Editorial acknowledgement
Legal entity responsible for the study
Faron Pharmaceuticals.
Funding
Faron Pharmaceuticals.
Disclosure
P. Bono: Financial Interests, Personal, Advisory Board: MSD, Oncorena, TILT Biotherapeutics, Faron Pharmaceuticals; Financial Interests, Personal, Full or part-time Employment, Chief Medical Officer: Terveystalo Finland; Financial Interests, Personal, Stocks/Shares: Terveystalo Finland; Financial Interests, Personal, Ownership Interest: TILT Biotherapeutics; Other, Stock ownership (spouse): Faron Pharmaceuticals. L. Verlingue: Financial Interests, Personal, Stocks/Shares, CEO of Resolved dedicated to treatment approval prediction: Resolved; Financial Interests, Institutional, Research Grant: Bristol Myers Squibb; Financial Interests, Institutional, Funding, Contract for bioinformatic analysis: Pierre Fabre, Servier; Non-Financial Interests, Advisory Role: Klineo; Non-Financial Interests, Institutional, Proprietary Information, As part of the Drug Development Department (DITEP) of Gustave Roussy and of the Phase 1 unit of Centre Léon Bérard, as medical doctor, LV report being: Principal/sub-Investigator of Clinical Trials for AbbVie, Adaptimmune, Aduro Biotech, Agios Pharmaceuticals, Amgen, Argen-X Bvba, Arno Therapeutics, Astex Pharmaceuticals, AstraZeneca Ab, Aveo, Basilea Pharmaceutica International Ltd., Bayer Healthcare Ag, Bbb Technologies Bv, BeiGene, Blueprint Medicines, Boehringer Ingelheim, Boston Pharmaceuticals, Bristol Myers Squibb, Ca, Celgene Corporation, Chugai Pharmaceutical Co, Clovis Oncology, Cullinan-Apollo, Daiichi Sankyo, Debiopharm, Eisai, Eisai Limited, Eli Lilly, Exelixis, Faron Pharmaceuticals Ltd., Forma Tharapeutics, Gamamabs, Genentech, GSK, H3 Biomedicine, F. Hoffmann-La Roche AG, Imcheck Therapeutics, Innate Pharma, Institut De Recherche Pierre Fabre, Iris Servier, Janssen Cilag, Janssen Research Foundation, Kura Oncology, Kyowa Kirin Pharm. Dev, Lilly France, Loxo Oncology, Lytix Biopharma A: Pharmas. M.J. De Miguel Luken: Financial Interests, Institutional, Invited Speaker: Janssen, MSD; Non-Financial Interests, Principal Investigator: Janssen, MSD, Roche, PharmaMar, Replimune, Novartis, AbbVie, Achilles, Amunix, Arcus, Furmo, BioNTech, Catalym, Dizal, Genentech, Loxo, Numab, Seagen. A. Pasanen: Financial Interests, Personal, Advisory Board: Gilead, Roche, Novartis, Varian, Incyte; Financial Interests, Personal, Invited Speaker: Roche, Janssen-Cilag, Incyte; Non-Financial Interests, Principal Investigator: Faron, Incyte. D. Robbrecht: Financial Interests, Personal, Advisory Board: Merck AG, Pfizer; Financial Interests, Institutional, Invited Speaker: AstraZeneca, Treatmeds, DUOS; Non-Financial Interests, Advisory Role: Bayer; Non-Financial Interests, Principal Investigator: Sanofi, Incyte, Roche, InteRNA, Numab Therapeutics, Menarini. T. Skyttä: Financial Interests, Personal, Invited Speaker: BMS, AstraZeneca; Financial Interests, Personal, Other, DMC: Faron; Financial Interests, Personal, Advisory Board: Novartis, Pierre Fabre, MSD; Financial Interests, Personal, Member of Board of Directors: Finnish Oncological Society. S.M.E. Iivanainen: Financial Interests, Personal, Advisory Board: MSD, BMS, Novartis, Roche; Financial Interests, Institutional, Invited Speaker: BMS, Faron; Financial Interests, Institutional, Research Grant: AstraZeneca, Roche; Financial Interests, Institutional, Other, Sub-investigator: MSD; Financial Interests, Personal and Institutional, Invited Speaker, The Origama study: Roche; Financial Interests, Institutional, Other, Sub-Investigator (The ECHO Trial): Kaiku Health; Other, Study Steering Committee Member: F. Hoffmann-La Roche. S. Shetty: Financial Interests, Personal, Other, Consultancy fees: Faron Pharmaceuticals; Financial Interests, Personal, Invited Speaker, Speaker fees for educational event: Eisai; Non-Financial Interests, Principal Investigator, UK coordinating investigator: Faron Pharmaceuticals. Y.T. Ma: Financial Interests, Personal, Advisory Board: Eisai, Roche, AstraZeneca, Ipsen; Financial Interests, Personal, Steering Committee Member: Faron; Financial Interests, Institutional, Local PI: Faron; Financial Interests, Institutional, Coordinating PI: QED. D.M. Graham: Financial Interests, Personal, Advisory Board, Consulting role on advisory board: clinigen; Financial Interests, Personal, Invited Speaker: Cancer Drug Development Fund; Financial Interests, Personal, Advisory Board: McCann Health; Financial Interests, Institutional, Invited Speaker, Institutional funding from study: MSD, Codiak Biosciences, Starpharma, Faron Pharmaceuticals, Synthon, Janssen; Financial Interests, Institutional, Other, Sub-I: Institutional funding from study: AstraZeneca, Roche, BerGenBio, GSK, Bayer, Bicycle pharmaceuticals, Carrick, Taiho pharmaceuticals, CytomX Therapeutics, RedX Pharma PLC, Eisai Inc, Octimet, Orion Pharma, Kinex pharmaceuticals, Boehringer Ingelheim, BMS, Turning Point Therapeutics, Immutep, Agalimmune, Kymab, Blueprint, Astellas, Cellcentric, UCB Biopharma USL, Eli Lily, Seagen, Repare therapeutics, Timepoint Therapeutics, Astex, Stemline, Crescendo Biologics Ltd., ADC Therapeutics, Genentech, Avacta Life Sciences Ltd., Nurix Therapeutics Inc; Financial Interests, Institutional, Other, Sub-I: Institutional finding from study: Chugai Pharmaceuticals; Financial Interests, Institutional, Invited Speaker: Incyte. S.P. Arora: Financial Interests, Personal, Invited Speaker: Exelixis, Bristol Myers Squibb; Financial Interests, Personal, Advisory Board: QED Therapeutics, AstraZeneca, Seagen; Financial Interests, Institutional, Local PI: Caris Life Sciences, Faron, Isofol, Ipsen, BeiGene, Tvardi, Novartis, Therabionic, Genentech; Non-Financial Interests, Member of Board of Directors: Support New India. P.M. Jaakkola: Financial Interests, Personal, Advisory Board: MSD, Ipsen. C. Yap: Financial Interests, Personal, Advisory Board, Statistical Consultant: Faron Pharmaceutical; Financial Interests, Personal, Invited Speaker, Speaker at a Training Workshop: Bayer; Financial Interests, Institutional, Research Grant: AstraZeneca, Celgene, Novartis; Financial Interests, Personal and Institutional, Research Grant: Faron Pharmaceuticals. M. Hollmén: Financial Interests, Personal, Full or part-time Employment, Chief Scientific Officer: Faron Pharmaceuticals; Financial Interests, Personal, Stocks/Shares: Faron Pharmaceuticals; Financial Interests, Institutional, Invited Speaker, Research agreement for the pre-clinical and clinical development of bexmarilimab: Faron Pharmaceuticals; Non-Financial Interests, Personal, Product Samples, Bexmarilimab (anti-Clever-1 antibody) and MATINS clinical trial patient material: Faron Pharmaceuticals. J.P. Koivunen: Financial Interests, Personal, Advisory Board: Merck Sharp Dome, BMS, AstraZeneca, Pfizer, Roche, Boehringer-Ingelheim, Takeda, Amgen; Financial Interests, Personal, Full or part-time Employment: Faron Pharmaceuticals; Financial Interests, Personal, Stocks/Shares: Faron Pharmaceuticals; Financial Interests, Institutional, Funding: AstraZeneca; Financial Interests, Institutional, Invited Speaker: Boehringer-Ingelheim, Roche. A.R. Minchom: Financial Interests, Personal, Other, Expenses: Amgen pharmaceuticals, Loxo Oncology; Financial Interests, Personal, Invited Speaker: Bayer Pharmaceuticals, Chugai Pharmaceuticls, GSK, Janssen Pharmaceuticals, Merck pharmaceuticals; Financial Interests, Personal, Advisory Board: Faron pharmaceuticals, Janssen Pharmaceuticals, Merck pharmaceuticals, Takeda, Genmab; Financial Interests, Personal, Expert Testimony: GSK; Financial Interests, Institutional, Other, Research funding: MSD, Merck Pharmaceuticals; Financial Interests, Personal, Other, Honoraria: Novartis Oncology.
Resources from the same session
710P - A retrospective study on the safety and adequacy of fresh biopsies for next generation sequencing in early-phase clinical trials
Presenter: Edoardo Crimini
Session: Poster session 17
711TiP - A phase I/II, first-in-human, open-label, dose-escalation study of TAK-186, an EGFR × CD3ε COBRA T cell engager, in adult patients with unresectable, locally advanced, or metastatic solid tumors
Presenter: Andrew Weickhardt
Session: Poster session 17
712TiP - A phase I/II multicenter, open-label, dose-escalation, safety, pharmacodynamic, and pharmacokinetic study of Q901 administered via intravenous infusion in adult patients with selected advanced solid tumors with a cohort expansion at the recommended phase II dose
Presenter: Angela Alistar
Session: Poster session 17
713TiP - A phase I study of PRT3789, a potent and selective degrader of SMARCA2 in patients with advanced or metastatic solid tumors and a SMARCA4 mutation
Presenter: Ibiayi Dagogo-Jack
Session: Poster session 17
714TiP - A phase Ia/Ib, first-in-human, dose-escalation study evaluating the safety, tolerability, and efficacy of IOS-1002, a LILRB1, LILRB2, and KIR3DL1 targeting HLA-derived fusion protein administered alone or in combination with a PD-1 antibody in patients with advanced solid tumors
Presenter: Stephen Luen
Session: Poster session 17
715TiP - ARTS-021-1001: Phase I/II study of ARTS-021, a potent, oral administrated, selective CDK2 inhibitor, in advanced or metastatic solid tumors
Presenter: Yan Wang
Session: Poster session 17
716TiP - DETERMINE: A pioneering UK precision medicine trial for rare cancers
Presenter: Gary Middleton
Session: Poster session 17
717TiP - An open-label, multicentre, dose-escalation, first-in-human phase I study to evaluate safety, tolerability and antineoplastic activity of OATD-02 (dual arginase 1 and arginase 2 inhibitor) in patients with selected advanced and/or metastatic solid tumors
Presenter: Marta Dudek
Session: Poster session 17
718TiP - DEKA-1 a dose-finding phase I trial: Observing safety and biomarkers using DK210 (EGFR) for inoperable locally advanced and/or metastatic EGFR+ tumors with progressive disease failing systemic therapy
Presenter: Elizabeth Moser
Session: Poster session 17
719TiP - A phase I/Ib study of the Werner (WRN) helicase inhibitor HRO761 as single agent and in combination with irinotecan or tislelizumab in patients with microsatellite instability-high (MSIhi) or mismatch repair deficient (dMMR) advanced solid tumors
Presenter: Michele Moschetta
Session: Poster session 17