Abstract 1029P
Background
Dazostinag (TAK-676) is a novel, IV, small molecule synthetic STimulator of INterferon Genes (STING) agonist, which acts as an innate immunity enhancer. In preclinical models, dazostinag induced dose-dependent cytokine production and activation/proliferation of immune cells. We present data from Part 1 of iintune-1 (NCT04420884), a phase 1 study of single agent (SA) dazostinag and combined with pembro in advanced or metastatic solid tumors.
Methods
Part 1 comprised a single-pt safety lead-in with SA dazostinag 0.1 mg IV, followed by dose escalation using Bayesian Logistic Regression Model design. Dose escalation in the combination arm began after no dose-limiting toxicities (DLTs) were seen with ≥2 SA doses. Pts receive dazostinag IV (Days 1, 8, 15) +/- pembro 200 mg IV (Day 1) in 21-day cycles.
Results
As of May 2023, 36 and 43 pts have received SA dazostinag and with pembro, respectively. There have been no DLTs up to 7 mg SA and 5 mg with pembro. The most common adverse events were fatigue (33%), nausea (29%), and pyrexia (22%). Dazostinag had linear PK across the dose range tested and was not affected by combination with pembro; elimination profile was bi-phasic with a terminal half-life of 0.5–1.7 hrs. Exposure-safety analysis indicated increasing incidence of fever or cytokine release syndrome with dazostinag Cmax. PK/PD analysis for all pts indicated dose/concentration-dependent increases in a blood 24-gene STING signature score, and plasma IFN-γ and IP-10. Dazostinag achieved a >3.5-fold induction of STING signature score across multiple dose levels. For dazostinag 5 mg with or without pembro, a >2-fold increase in IFN-γ and other cytokines (including IP-10) and increased peripheral Ki67+CD8+ T cell proliferation were observed. Three pts had objective confirmed clinical responses with dazostinag plus pembro.
Conclusions
Preliminary safety, PK/PD data, and anti-tumor activity support the declaration of the RDE of dazostinag 5 mg + pembro 200 mg. Expansion cohorts in colorectal and head and neck cancer are enrolling.
Clinical trial identification
NCT04420884.
Editorial acknowledgement
Medical writing, under the direction of the authors, was provided by Philippa Lloyd, BSc, of Ashfield MedComms, an Inizio company, funded by Takeda Pharmaceuticals, U.S.A., Inc., Lexington, MA, and complied with GPP guidelines (DeTora LM, et al. Ann Intern Med 2022 ;175:1298–1304).
Legal entity responsible for the study
Takeda Development Center Americas, Inc. (TDCA), Lexington, MA, USA.
Funding
Takeda Development Center Americas, Inc. (TDCA), Lexington, MA, USA
Disclosure
A.J. Olszanski: Financial Interests, Personal, Advisory Board: Merck, Pfizer, BMS. J.J. Luke: Financial Interests, Personal, Other, DSMB: AbbVie, Agenus, Evaxion; Financial Interests, Personal, Funding, DSMB: Immutep; Financial Interests, Personal, Advisory Board: 7 Hills, Affivant, BioCytics, Bright Peak, Exo, Fstar, Inzen, RefleXion, Xilio (stock) Actym, Alphamab Oncology, Arch Oncology, Duke Street Bio, Kanaph, Mavu, NeoTx, Onc.AI, OncoNano, physIQ, Pyxis, Saros, STipe, Tempest; Financial Interests, Personal, Speaker, Consultant, Advisor, Consultancy: AbbVie, Agenus, Alnylam, AstraZeneca, Atomwise, Bayer, Bristol Myers Squibb, Castle, Checkmate, Codiak, Crown, Cugene, Curadev, Day One, Eisai, EMD Serono, Endeavor, Flame, G1 Therapeutics, Genentech, Gilead, Glenmark, HotSpot, Kadmon, KSQ, Janssen, Ikena; Financial Interests, Institutional, Research Funding: AbbVie, Astellas, AstraZeneca, Bristol Myers Squibb, Corvus, Day One, EMD Serono, Fstar, Genmab, Hot Spot, Ikena, Immatics, Incyte, Kadmon, KAHR, Macrogenics, Merck, Moderna, Nektar, Next Cure, Numab, Palleon, Pfizer, Replimmune, Rubius, Servier, Scholar . P. Lorusso: Financial Interests, Personal, Other, Honoraria: Five Prime Therapeutics; Financial Interests, Personal, Advisory Role: AbbVie, ABL Bio, Agenus, Agios, Astellas Pharma, AstraZeneca, BAKX Therapeutics, CytomX Therapeutics, EMD Serono, Five Prime Therapeutics, Genentech, Genmab, GSK, Halozyme, I-Mab, ImCheck therapeutics, ImmunoMet, IQvia, Kineta, Kyowa Kirin International, Macrogenics, Mekanistic Therapeutics, Molecular Templates, Pfizer, QED Therapeutics, Relay Therapeutics, Roche/Genentech, Salarius Pharmaceuticals, Seagen, Shattuck Labs, Silverback Therapeutics, SK Life Sciences, Sotio, ST Cube, Stemline Therapeutics, Takeda, Trial to Reduce IDDM in the Genetically at Risk (TRIGR), TYME, Zentalis; Financial Interests, Institutional, Research Funding: Genentech; Financial Interests, Personal, Other, Travel, accommodations, expenses: Genentech. G.S. Falchook: Financial Interests, Personal, Royalties: Wolters Kluwer; Financial Interests, Institutional, Advisory Role: AbbVie, Fujifilm, Silicon, Navire, Turning Point, Predicine, Inspirna, Regeneron, Jubilant, BostonGene, Teon, Merck; Financial Interests, Personal, Advisory Role: EMD Serono; Financial Interests, Personal, Other, Speakers honorarium for CME: Total Health Conferencing, Rocky Mountain Oncology; Financial Interests, Personal, Other, Travel (self, for work and/or research related to institution): Amgen (2022), Bristol Myers Squibb (2015), EMD Serono (2011, 2012, 2013), Fujifilm (2018), Millennium (2013), Sarah Cannon Research Institute (employer, at least once yearly), Synthorx /Sanofi (2022); Financial Interests, Institutional, Research Funding: 3-V Biosciences, Abbisko, AbbVie, ABL Bio, ADC Therapeutics, Accutar, Agenus, Aileron, American Society of Clinical Oncology, Amgen, ARMO/Eli Lilly, Artios, AstraZeneca, Bayer, BeiGene, Bioatla, Bioinvent, Biothera, Bicycle, Black Diamond, Boehringer Inge. P.L. Bedard: Financial Interests, Personal, Advisory Role: Seattle Genetics, Lilly, Amgen, Merck, Gilead Sciences, Zymeworks, Repare Therapeutics; Financial Interests, Institutional, Advisory Role: BMS, Pfizer; Financial Interests, Institutional, Research Funding: Bristol Myers Squibb, Sanofi, AstraZeneca, Genentech/Roche, GSK, Novartis, Merck, Seattle Genetics, Lilly, Amgen, Bicara, Zymeworks, Medicenna, Bayer, Takeda. R.E. Sanborn: Financial Interests, Personal, Invited Speaker: Targeted Oncology, GameOn!, OncLive; Financial Interests, Personal, Writing Engagement: EMD Serono; Financial Interests, Personal, Advisory Board: EMD Serono, Daiichi Sankyo, Lilly Oncology, Janssen Oncology, Macrogenics, Sanofi/Aventis, Regeneron, Mirati Therapeutics, GSK, Illumina, G1 Therapeutics, AstraZeneca; Financial Interests, Personal, Research Grant, Funding for investigator-initiated trials: AstraZeneca, Merck. S.P. Patel: Financial Interests, Personal, Advisory Board: Amgen, AstraZeneca, Bristol Myers Squibb, Certis, Eli Lilly, Jazz, Genentech, Illumina, Merck, Pfizer, Rakuten, Tempus; Financial Interests, Personal, Research Grant: Amgen, AstraZeneca/MedImmune, Bristol Myers Squibb, Eli Lilly, Fate Therapeutics, Gilead, Iovance, Merck, Pfizer, Roche/Genentech, SQZ Biotechnologies. J.P. Gibbs: Financial Interests, Personal, Full or part-time Employment: Takeda; Financial Interests, Personal, Stocks/Shares: Takeda. C. Li: Financial Interests, Personal, Full or part-time Employment: Takeda Pharmaceuticals; Financial Interests, Personal, Stocks/Shares: Takeda Pharmaceuticals. Y. Huang: Financial Interests, Personal, Full or part-time Employment: Takeda; Financial Interests, Personal, Stocks/Shares: Takeda. R. Gregory: Financial Interests, Personal, Full or part-time Employment: Takeda; Financial Interests, Personal, Stocks/Shares: Takeda. S. Perera: Financial Interests, Personal, Stocks/Shares: Takeda Pharmaceutical; Financial Interests, Personal, Full or part-time Employment: Takeda. R. Xu: Financial Interests, Personal, Full or part-time Employment: Takeda Development Center Americas. A. Joshi, M.Y. Lee, J. Raizer: Financial Interests, Personal, Full or part-time Employment: Takeda; Financial Interests, Personal, Stocks/Shares: Takeda. X. Gao: Financial Interests, Institutional, Principal Investigator: Arvinas, Exelixis, Pfizer, Harpoon Therapeutics, Aprea Therapeutics, Aravive, Merck, Poseida Therapeutics, TopAlliance Biosciences, Novartis, Regeneron, Bayer, ALX Oncology; Financial Interests, Personal, Advisory Board: Bayer, Guardant Health, Flare Therapeutics, Silver Therapeutics, PureTech Health, Myovant Sciences, PathAI. All other authors have declared no conflicts of interest.
Resources from the same session
1048P - Phase I/II Study of JK08, an IL-15 antibody fusion protein targeting CTLA-4, with unresectable locally advanced or metastatic cancer
Presenter: Nuria Kotecki
Session: Poster session 19
1049P - Phase Ib/II trial of envafolimab, a novel subcutaneous single-domain anti-PD-L1 monoclonal antibody, plus lenvatinib in patients with selected advanced solid tumors
Presenter: Tianshu Liu
Session: Poster session 19
1050P - Sensitization to immunotherapy through manipulation of tumor transcription by lurbinectedin
Presenter: Joan Russo-Cabrera
Session: Poster session 19
1051P - Intratumoral injection of LTX-315 in combination with pembrolizumab in patients with advanced melanoma refractory to prior PD-1/PD-L1 therapy: Interim results from the ATLAS-IT-05 trial
Presenter: Stephane Dalle
Session: Poster session 19
1052P - Phase-Ib trial of metformin combined with nivolumab for refractory/recurrent solid tumors
Presenter: Toshio Kubo
Session: Poster session 19
1053P - Tumor-restricted delivery of an immune-therapeutic payload by modified macrophages for the treatment of glioblastoma: The TEM-GBM STUDY (NCT03866109)
Presenter: Fabio Ciceri
Session: Poster session 19
1054P - A phase Ia study to evaluate the safety, tolerability, pharmacokinetics and preliminary efficacy of a modular CLDN18.2-targeting PG CAR-T therapy (IBI345) in patients with CLDN18.2+ solid tumors
Presenter: Songbing Qin
Session: Poster session 19
1055P - Safety and Activity of SmarT cells plus PD-1 blocking antibodies in patients with heavily pretreated solid cancers: An open-label and dose-escalation study
Presenter: Qin Liu
Session: Poster session 19
1056P - Efficacy of spartalizumab across multiple cancer types in patients with PD1-high mRNA expressing tumors (SOLTI-1904 ACROPOLI)
Presenter: Aleix Prat
Session: Poster session 19
1057P - Long-term follow-up of a phase II study of tislelizumab (TIS) monotherapy in patients (pts) with previously treated, locally advanced, unresectable or metastatic microsatellite instability-high (MSI-H) or mismatch repair-deficient (dMMR) solid tumors
Presenter: Jian Li
Session: Poster session 19