Direkt zum Seiteninhalt, zur Hauptnavigation, zur Unternavigation, zur Fußzeile.

-- 12 November 2012
immatics appoints Peter Chambré as Chairman
-- 08 November 2012
immatics’ renal cancer vaccine IMA901 completes phase 3 patient recruitment and is granted US orphan drug designation by the FDA
-- 27 September 2012
IMA950 Phase I results presented by Allan James at ESMO 2012 (Sept. 30) in Vienna
-- 28 August 2012
IMA950 data presented by Roy Rampling at EANO 2012 (Sept. 7) in Marseille
-- 29 July 2012
immatics announces publication of IMA901 cancer vaccine data in Nature Medicine: immune response associates with longer survival
-- 01 June 2012
immatics presents encouraging overall survival data from a phase 2 study in Advanced Colorectal Cancer at the ASCO Annual Meeting
-- 25 May 2012
immatics presenting at ASCO Annual Meeting 2012 (June 1-5) in Chicago
-- 25 May 2012
immatics wins 2012 TiE50 Award
-- 22 May 2012
immatics at CIMT Annual Meeting 2012 starting tomorrow in Mainz, Germany
-- 03 May 2012
Harpreet Singh, CSO at immatics, will present at Immunotherapy Leaders’ Forum 2012 (May 9-11) in Barcelona, Spain
-- 19 April 2012
Paul Higham, CEO at immatics, will present at BioTrinity 2012 (April 24-26) in Newbury, Berkshire, UK
-- 12 April 2012
immatics appoints Dr Rainer Kramer as Chief Business Officer
-- 01 April 2012
immatics and collaborators publish preclinical results for Glioma Vaccine IMA950 in "Brain"
-- 24 January 2012
immatics presents positive Phase II results with its therapeutic cancer vaccine IMA910 in patients with advanced colorectal cancer at the ASCO Gastrointestinal Cancers Symposium

08 November 2012

immatics’ renal cancer vaccine IMA901 completes phase 3 patient recruitment and is granted US orphan drug designation by the FDA

immatics biotechnologies GmbH, a biopharmaceutical company developing rationally designed therapeutic vaccines that are active against cancer, announced today that it has completed patient recruitment into the pivotal phase 3 trial evaluating its lead cancer vaccine IMA901 for renal cell carcinoma (RCC). The trial has completed patient inclusion and it is expected that around 345 patients will be randomized across 10 countries in the US and Europe. The first (interim) overall survival results are expected during the first half of 2014.

The phase 3 IMPRINT trial* is designed to show an overall survival benefit with IMA901 in combination with sunitinib (Sutent®, Pfizer), standard first-line therapy in comparison to sunitinib alone in patients with metastatic and/or locally advanced RCC. The secondary endpoints include immune response to the peptides contained in IMA901, progression-free survival, safety and tolerability.

The study aims to build on the promising survival and immune response data observed in the phase 2 study with IMA901 in advanced RCC patients. These data show that patients who produced an immune response to two or more of the tumor-associated peptides (TUMAPs) contained in IMA901 had a significantly longer survival. Key data from the scientific and clinical development of IMA901 were recently published in Nature Medicine.**

Chief investigator of the trial is Professor Brian Rini, Lerner College of Medicine, Department of Solid Tumor Oncology at the Cleveland Clinic Taussig Cancer Institute, Cleveland, Ohio. The European lead investigator is Professor Tim Eisen, Clinical Director of Medical Oncology at Addenbrooke’s Hospital, University of Cambridge, UK.

Dr. Carsten Reinhardt, CMO of immatics, said: “We have achieved another key milestone in immatics’ development. The rate of patient recruitment in this pivotal trial with IMA901 reflects a very high level of interest in this novel cancer vaccine for the treatment of renal cell carcinoma both by investigators and also patients. IMA901, which contains multiple highly relevant tumor peptides, has already indicated the potential to extend patient survival and we look forward to this being confirmed in this pivotal trial.”

US orphan drug designation for IMA901

In addition, immatics announced today that IMA901 has been granted orphan drug designation from the US Food and Drug Administration (FDA) for the treatment of renal cell carcinoma in HLA-A*02 positive patients. The FDA grants orphan drug designation to novel drugs aimed at treating rare diseases or conditions.

Paul Higham, CEO of immatics, added: “IMA901 has been rationally designed to redirect the immune system to make it recognize and control tumors. We believe that our vaccines could deliver a step-change in the treatment of cancer patients, allowing them to live longer with their cancer while maintaining their quality of life. We are delighted with the orphan drug designation and look forward to reviewing the initial overall survival and immune response results from this phase 3 study in the first half of 2014 and the final data in 2015.”   

* IMPRINT = IMA901 MultiPeptide vaccine Randomized INTernational study
** “Multipeptide immune response to cancer vaccine IMA901 after single-dose cyclophosphamide associates with longer patient survival,” Walter S., Weinschenk T. et al. (2012) Nature Medicine. Published online: 29 July 2012
[Free pdf copy of the article]


For additional information please contact us via email or call +49 (7071) 5397-0.

-/ 12_IMM_06_immatics' IMA901 completes phase 3 patient recruitment and is granted US orphan drug designation (PDF, 94 KB)

-/ 12_IMM_06_immatics' Nierenkrebsimpfstoff IMA901 beendet Patientenrekrutierung der Phase 3-Studie und bekommt Zulassung als Orphan Drug von der FDA (PDF, 104 KB)