Immatics N.V. (IMTX)
Immatics N.V. is a clinical-stage biopharmaceutical firm dedicated to discovering and advancing T-cell receptor (TCR) based immunotherapies aimed at combating cancer, primarily within the United States. Its therapeutic strategy centers on targeted immunotherapies for solid tumors, utilizing two distinct approaches: adoptive cell therapies (ACT) and antibody-like TCR Bispecifics. The company's ACTengine™ portfolio features several candidates in Phase I clinical trials. These include IMA201, designed to recognize melanoma-associated antigens 4 or 8 in solid tumor patients; IMA202, which targets melanoma-associated antigen 1 across various solid tumor types, such as squamous non-small cell lung carcinoma and hepatocellular carcinoma; and IMA203, aimed at preferentially expressed antigen in melanoma in adult patients with recurrent or treatment-resistant solid tumors. Additionally, IMA204, currently in preclinical stages, focuses on targeting tumor stroma cells. In its preclinical TCR Bispecifics pipeline, Immatics is advancing IMA401, which targets cancer testis antigens for solid tumor indications, and IMA402, also under investigation for solid tumor therapies. Other programs include IMA101 for cancer treatment and IMA301, an allogeneic cellular therapy candidate. Immatics has established strategic partnerships to bolster its development efforts. These include collaborations with GlaxoSmithKline Intellectual Property Development Limited for novel adoptive cell therapies across various cancer indications; MD Anderson Cancer Center for multiple T-cell and TCR-based adoptive cellular therapies; Celgene Switzerland LLC for additional novel adoptive cell therapies; and Genmab A/S to develop T-cell engaging bispecific immunotherapies for diverse cancer indications. The company's headquarters are situated in Tübingen, Germany.
Sector: Biological Products, (No Diagnostic Substances)
Industry: Biotechnology
Immatics N.V.
Trials need funding. See this company's dilution risk and cash position.
- Phase 3Completed
IMA901 in Patients Receiving Sunitinib for Advanced/Metastatic Renal Cell Carcinoma
Sunitinib, GM-CSF
Metastatic Renal Cell Carcinoma
NCT01265901Enrollment339StartDec 2010Primary CompletionJul 2015CompletionJul 2015 - Phase 3Recruiting
SUPRAME-ACTengine® IMA203 vs. Investigator's Choice of Treatment in Previously Treated, Unresectable or Metastatic Cutaneous Melanoma
IMA203, nivolumab plus relatlimab
Melanoma, Cutaneous Malignant, Mucosal Melanoma
NCT06743126Enrollment450StartJan 2025Primary CompletionJan 2028est.CompletionAug 2032est. - Phase 2Completed
IMA901 in Advanced Renal Cell Carcinoma Patients With Measurable Disease
Endoxana, IMA901, Leukine, IMA901 and Leukine
Renal Cell Carcinoma
NCT00523159Enrollment68StartMay 2007Primary CompletionAug 2009CompletionAug 2009 - Phase 1/2Completed
IMA910 Plus GM-CSF With Low-dose Cyclophosphamide Pre-treatment in Advanced Colorectal Carcinoma Patients Following a Successful 12 Week First-line Treatment With Oxaliplatin-based Chemotherapy (IMA910-101)
Endoxana, Leukine, IMA910, Endoxana, Leukine, IMA910, Aldara
Colorectal Carcinoma
NCT00785122Enrollment92StartJun 2008Primary CompletionJan 2011CompletionMay 2013 - Phase 1/2Recruiting
ACTengine® IMA203/IMA203CD8 as Monotherapy or in Combination With Nivolumab in Recurrent and/or Refractory Solid Tumors
IMA203 Product, IMA203 product- flat dose
Refractory Cancer, Recurrent Cancer +2
NCT03686124Enrollment375StartMay 2019Primary CompletionDec 2028est.READOUTCompletionJun 2032est. - Phase 1/2Recruiting
IMA402 T Cell-Engaging Receptor Molecule (TCER®) in Recurrent and/or Refractory Solid Tumors
IMA402, IMA402 and checkpoint inhibitor
Refractory Cancer, Recurrent Cancer +2
NCT05958121Enrollment400StartAug 2023Primary CompletionSep 2027est.READOUTCompletionSep 2027est. - Phase 1Terminated
Peptide-based Glioma Vaccine IMA950 in Patients With Glioblastoma
Cyclophosphamide, IMA950 plus GM-CSF
Glioblastoma
NCT01403285Enrollment6StartAug 2011Primary CompletionApr 2014CompletionApr 2014 - Phase 1Completed
GAPVAC Phase I Trial in Newly Diagnosed Glioblastoma Patients
APVAC1 vaccine plus Poly-ICLC and GM-CSF, APVAC2 vaccine plus Poly-ICLC and GM-CSF
Glioblastoma
NCT02149225Enrollment16StartOct 2014Primary CompletionJun 2018CompletionJun 2018 - Phase 1Completed
ACTolog in Patients With Solid Cancers
Fludarabine, Cyclophosphamide
Cancer, Solid Tumor
NCT02876510Enrollment38StartJun 2017Primary CompletionSep 2021CompletionSep 2021 - Phase 1Completed
TCR-engineered T Cells in Solid Tumors (ACTengine IMA201-101)
IMA201 Product
Solid Tumor, Cancer +2
NCT03247309Enrollment7StartDec 2018Primary CompletionApr 2023CompletionSep 2023 - Phase 1Completed
TCR-engineered T Cells in Solid Tumors: IMA202-101
IMA202 Product
Solid Tumor, Adult, Refractory Cancer +2
NCT03441100Enrollment16StartMay 2019Primary CompletionJun 2022CompletionMar 2023 - Phase 1Active, not recruiting
IMA401 TCER® in Recurrent and/or Refractory Solid Tumors, Alone or in Combination With a Checkpoint Inhibitor
IMA401 (Phase Ia), Pembrolizumab (Phase Ia)
Refractory Cancer, Recurrent Cancer +2
NCT05359445Enrollment95StartMay 2022Primary CompletionMar 2026CompletionDec 2029est. - Phase 1Recruiting
ACTengine® IMA203 Combined With mRNA-4203
IMA203, mRNA-4203
Cutaneous Melanoma, Synovial Sarcoma
NCT06946225Enrollment15StartJul 2025Primary CompletionAug 2029est.CompletionAug 2029est. - ObservationalCompleted
Human Leukocyte Antigen Typing and Tumor Antigen Expression Profiling
-
Refractory Cancer, Recurrent Cancer +2
NCT03760952Enrollment242StartFeb 2019Primary CompletionNov 2022CompletionNov 2022
| Drug / Therapy | Link | ||
|---|---|---|---|
| Phase 3 | Completed | Sunitinib, GM-CSF | NCT01265901 |
| Phase 3 | Recruiting | IMA203, nivolumab plus relatlimab | NCT06743126 |
| Phase 2 | Completed | Endoxana, IMA901, Leukine, IMA901 and Leukine | NCT00523159 |
| Phase 1/2 | Completed | Endoxana, Leukine, IMA910, Endoxana, Leukine, IMA910, Aldara | NCT00785122 |
| Phase 1/2 | Recruiting | IMA203 Product, IMA203 product- flat dose | NCT03686124 |
| Phase 1/2 | Recruiting | IMA402, IMA402 and checkpoint inhibitor | NCT05958121 |
| Phase 1 | Terminated | Cyclophosphamide, IMA950 plus GM-CSF | NCT01403285 |
| Phase 1 | Completed | APVAC1 vaccine plus Poly-ICLC and GM-CSF, APVAC2 vaccine plus Poly-ICLC and GM-CSF | NCT02149225 |
| Phase 1 | Completed | Fludarabine, Cyclophosphamide | NCT02876510 |
| Phase 1 | Completed | IMA201 Product | NCT03247309 |
| Phase 1 | Completed | IMA202 Product | NCT03441100 |
| Phase 1 | Active, not recruiting | IMA401 (Phase Ia), Pembrolizumab (Phase Ia) | NCT05359445 |
| Phase 1 | Recruiting | IMA203, mRNA-4203 | NCT06946225 |
| Observational | Completed | - | NCT03760952 |