Novel T-cell Targets for Cancer Immunotherapies Immatics Biotechnologies, Germany Texas FreshAir Conference Houston, October 23, 2014 Dr. Harpreet Singh Co-founder and Chief Scientific Officer This presentatio is n intended solely for evaluation of investment opportunities.. © 2014 immatics biotechnologies GmbH. Not for further reproduction or distribution. Immatics Biotechnologies (Germany) An established company dedicated to off-the-shelf cancer immunotherapies Founded in 2000 as a spin-out from the University of Tuebingen, Germany by Harpreet Singh, Toni Weinschenk, Hans-Georg Rammensee et al. Since 2004 Immatics Biotechnologies GmbH has: Raised € 142m (~$180m) in four financing rounds plus ~€ 10m public funding Established and continuously evolved its proprietary technology platform XPRESIDENT® Built a robust pipeline with three off-the-shelf cancer vaccines in clinical development With lead product IMA901 (Renal Cell Cancer) in phase 3 trial (in collaboration with Pfizer) A number of preclinical candidates partnered with Roche immatics key facts: Proprietary antigen discovery platform Strong IP protection technology and on all assets Experienced management team Strong investor base in Europe (family offices, venture capital) Based in Germany (HQ in Tuebingen) employing 80 FTEs 2 HLA-presented tumor-associated peptides (TUMAPs) The cancer immunopeptidome Our mission: Mapping the human immunopeptidome as centrally relevant information for all T-cell based immunotherapies. T cell Peptide HLA Immunopeptidome Protein Proteome G U A A C C U G G C A C A U U G A C C U G Tumor Cell 3 A C C G U A C A mRNA DNA A C A Genome / Transcriptome HLA-presented tumor associated-peptides (TUMAPs) Novel targets for T cells and TCR-based/like drugs Targets for vaccines and adoptive cellular therapy Targets for mAbs/sTCRs TCR-like Antibody T cell Soluble T-cell receptor Anti-CD3 sTCR G U G U A A A C C U G A C C G G U A C C A U G U G A U C A C A C U G A C C A C A G C U G A C A U A C C G U A C A 4 U G A C A A C C XPRESIDENT® Discovery Platform XPRESIDENT® Target Discovery Platform Unique features 6 Access to naturally presented targets for immunotherapy the cancer immunopeptidome Discovered on primary tumor tissues = real cancer cells No artificial cell lines, no computer algorithm-based predictions Immatics‘ immunopeptidome database – unique features Largest in size Quantitative data Human Immunopeptidome Program initiated in 2014 up to 3000 novel targets to be filed in patent applications in 15 different tumor types Including cancer and normal tissues Results in proprietary targets In contrast to others offering immunotherapies directed towards public targets XPRESIDENT™ Discovery Platform: Selection Process Month 0 Screen Month 12 – Hit – Lead – Drug Candidate 99 % 1. Shotgun Identification 2. Overexpression/ overpresentation analysis Month 24 Pre-clinical Development 0.7 % 0.2 % 5. Pharmaceutical characterization 50 % 7. GMP manufacturing 6. In vitro immunogenicity testing 50% 8. Filing of IMPD/IND 3. Functional considerations 4. IP/FTO analysis 30-90 interesting TUMAPs 10-20,000 non-redundnant peptides found on selected type of cancer (TUMAPs) 7 Phase 1 confidential ~10-30 validated TUMAPs Product candidate comprising 10-15 TUMAPs immatics Clinical Vaccine Pipeline Cancer Indication Discovery/ Pre-clinical Phase 1 Renal Cell Cancer A*02 (RCC) IMA910 Glioma A*02 (GB) IMA950 IMA942 Partnered with Lung Cancer A*02/A*24 (NSCLC) IMA932 Partnered with Prostate Cancer A*02/A*24 (PC) IMA962 Partnered with Phase 3 MAA/BLA In collaboration with IMA901 Colorectal Cancer A*02 (CRC) Gastric Cancer A*02/A*24 (GC) Phase 2 Partnered with IMA901 Renal Cell Cancer Vaccine Single-dose CY associated with improved survival (and reduced regulatory T cells) Breadth of immune response associated with improved survival XPRESIDENT® Discovery Platform Melanoma Renal Cell Cancer Colorectal Cancer Breast Cancer Pancreatic Cancer Glioma Bladder Cancer Gastric Cancer Urethral TC Cancer Non-small cell lung Cancer Ovarian Cancer Prostate Cancer Testis Cancer Liver Cancer Clinical or near-clinical stage CLL Drug discovery stage Feasibility stage Rheumatoid Arthritis AML adipose tissue adrenal gland artery bone marrow brain, whole breast colon esophagus gallbladder heart kidney leukocytes liver lung lymph node ovary pancreas placenta prostate salivary gland skeletal muscle skin small intestine spleen stomach testis thymus thyroid trachea urinary bladder uterine cervix uterus vein GC2215T GC2230T GC2234T GC2419T GC2423T GC2424T GC2426T GC2427T GC2428T GC2430T GC2432T GC2433T GC2435T GC2436T GC2437T GC2447T GC2448T GC2449T GC2451T GC2461T GC2466T GC305T GC701T GC702T GC703T GC704T GC705T GC766T GC767T GC772T GC772T GC775T GC799T healthy tissue 2.3 5.7 gastric cancer 6.1 7.5 8.0 5.7 10.6 13.9 13.9 13.9 13.0 19.7 18.4 16.0 13.9 21.1 26.0 Tumor-specific alternative splicing described in literature results into inclusion of a particular exon from which this peptide is derived 19.7 18.4 17.1 19.7 17.1 17.1 14.9 13.9 12.1 11.3 11.3 11.3 10.6 9.8 8.6 8.6 8.0 7.5 6.5 6.1 5.7 6.1 4.9 8.0 8.6 7.5 5.7 4.6 3.5 2.8 2.1 3.5 2.1 1.1 2.6 7.5 6.5 4.9 5.3 3.7 2.6 2.8 1.0 0.2 1.1 1.1 0.7 1.6 relative expression 29.9 P P P A A P P P P P P A M P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P P Example 1: Cancer-specific splicing Example 1: Cancer-specific splicing antigen Type IV Collagen Alpha-3 Chain (COL6A3)-restricted peptide 12 COL6A3 encodes the alpha-3 chain of type VI collagen, a component of the extracellular matrix Cancer-specific splicing of COL6A3 has been described for colon, bladder, prostate, and pancreatic cancer COL6A3 levels are increased in response to cisplatin in tumors. Endotrophin, a cleavage product of COL6A3, causes cisplatin resistance through induction of epithelial-mesenchymal transition Peptide COL6A3-002 (HLA-A*02-restricted) derived from cancer-specific exon 6 identified by XPRESIDENT® on 60 cancer samples from several entities (including pancreatic, NSCLC, colorectal, gastric cancer), but not on any normal tissue (N>120 covering different organ classes) Figure below: COL6A3 presentation on three PC tumor tissues compared to various healthy tissues (left panel) and grouped analyses of healthy tissues and different tumor types (right panel). Insert in left panel showing exemplary data of in vitro-primed COL6A3-002 specific T cells from HLA-A*02-positive and -negative healthy donors, the first step required to generate TCRs to this target and Boxplot of RPKM values for tumor (T) and autologous normal (N) tissues (N=29, TCGH research network) showing tumor-specific expression of the exon 6 (middle). Example 2: Organ-specific genes vs. antigens Differential mRNA expression vs. peptide presentation Peptide presentation in liver and HCC undisclosed liver-specific target Fibrinogen mRNA expression 13 mRNA expression Peptide presentation in HCC only Example 3: Tumor-associated, lowabundance antigens 14 Example 4: Mutated peptides Validation of NGS-identified mutations with Mass Spec 15 Actively Personalized Vaccines (APVACs) 17 Glioma Actively Personalized Vaccine Consortium GAPVAC • Establish an actively personalized vaccination (APVAC) approach for treatment of glioblastoma patients • Consortium with 14 partners funded by EU FP7 with € 6 mn • Coordinator: Immatics • Chief Investigator: Wolfgang Wick (Heidelberg) • Up to 30 glioblastoma patients treated with warehouse and mutanomederived APVACs • Approval by German Reg. Authority to start clinical phase I study received started in October 2014 XPRESIDENT®-derived Warehouse Approach XPRESIDENT®-derived Warehouse Approach Peptide Warehouse HLA/peptide multimer warehouse TCR Warehouse APVAC ACTolog ACTengine Actively Personalized Vaccines Adoptive Cellular Therapy with endogenous T cells Adoptive Cellular Therapy with engineered T cells Cassian Yee Patrick Hwu Willem Overwijk Laurence Cooper CONTACT immatics biotechnologies GmbH Paul-Ehrlich-Str. 15 72076 Tuebingen, Germany Phone +49-7071-5397-0 Fax +49-7071-5397-900 www.immatics.com info@immatics.com Thank you This is a confidential presentation intended solely for internal use. © 2014 immatics biotechnologies GmbH. Confidential. Not for further reproduction or distribution. Intellectual Property Processes & technologies • • • • XPRESIDENT® Formulation Methods of treatment TKIs + Vaccines Specific pharmaceutical compositions (e.g. multipeptide vaccine products) IMA901 (RCC) IMA910 (CRC) Substance-of-matter • TUMAPs (peptides) • mAbs and sTCRs • Corresponding nucleic acids • Biological products IMA942 (GC) IMA950 (GBM)