Immutep Ltd · ASX:IMM

Immutep — Prima BioMed — Shareholder Meeting (August 2015)

16 slides from Immutep's shareholder meeting presentation, Aug 5, 2015

  1. Slide 1: CEO Presentation Extraordinary General Meeting

    ASX:PRR; NASDAQ:PBMD; ISIN:US74154B2034 CEO Presentation Extraordinary General Meeting Marc Voigt, Chief Executive Officer July 31, 2015 Sydney, Australia Exhibit 99.1

  2. Slide 2: Notice: Forward Looking Statements

    Notice: Forward Looking Statements The purpose of the presentation is to provide an update of the business of Prima BioMed Ltd ACN (ASX:PRR; NASDAQ:PBMD; Deutsche Börse:YP1B.DE). These slides have been prepared as a presentation aid only and the information they contain may require further explanati

  3. Slide 3: Prima BioMed

    Prima BioMed • Clinical development of immuno-oncology products • Diversified portfolio with LAG-3 programs: Front positioning in growing immuno-oncology revolution of cancer treatment Mission: Emerging leader in immuno-oncology

  4. Slide 4: Prima's development since last AGM

    Prima‘s development since last AGM • Acquisition of well - positioned biotech company Immutep closed in Dec 2014 • Strengthening of management team • GSK milestone payment • Completion of CAN-003 trial with promising OS data • Consolidating clinical development of CVac and focus on promising LAG-3 t

  5. Slide 5: Development of the stock since last AGM

    Development of the stock since last AGM

  6. Slide 6: i © PRIMA BIOMED

    i © PRIMA BIOMED

  7. Slide 7: IMP321 clinical development

    IMP321 clinical development • Chemoimmunotherapy Phase IIb trial in metastatic breast cancer Approx. patients IMP321 with paclitaxel vs. paclitaxel and placebo Plan to start Q4 2015 • Phase I in immuno-oncology combination Planning phase of exciting combination study Scientific advice from EMA recei

  8. Slide 8: IMP321: AIPAC Study Design

    IMP321: AIPAC Study Design • Multicenter, randomized, double blind, Phase IIb study • Up to 200 patients with metastatic breast cancer • Treatment: first line paclitaxel + IMP321 / placebo • Primary objective: efficacy (as Progression-Free Survival) • Initiation after open-label, safety run-in phase

  9. Slide 9: IMP321: Potential Immuno-oncology combination

    IMP321: Potential Immuno-oncology combination Study Design • Multicenter, open label, dose escalation, Phase I study • Planning up to 30 patients with unresectable or metastatic cancer indication with dose escalation • Treatment: Checkpoint inhibitor + IMP321 • Primary objective: safety, tolerabilit

  10. Slide 10: IMP731 for autoimmune diseases

    IMP731 for autoimmune diseases • Dec. 2010. GlaxoSmithKline licensed from Immutep, rights to develop LAG-3 depleting antibodies for autoimmune disease - 64m total deal package (~A$118m) + royalties • GSK2831781 is currently in first time in human clinical trials (see NCT02195349 at clinicaltrials.go

  11. Slide 11: IMP701 is partnered with Novartis

    IMP701 is partnered with Novartis • IMP701 is an anti-LAG-3 antibody which blocks LAG-3-mediated immune down-regulation • 2012: US biotech CoStim licensed LAG-3 antagonists for cancer from Immutep • Feb. 2014: Novartis bought CoStim for undisclosed sum • Phase I expected to start soon

  12. Slide 12: CVac update

    CVac update • CAN-003 – Clear target patient population: in 2nd remission (CR2) of ovarian cancer – Overall Survival Data with positive trend in CR2: >16 months benefit :42Mo CVac vs 25.53Mo OSC – Progression free survival data: >8 months benefit: 12.91Mo for CVac versus PFS=4.94Mo for OSC – Favorab

  13. Slide 13: Outlook FY2016

    OUTLOOK FY2016

  14. Slide 14: Funding & cost savings

    Funding & cost savings Cash position at 30 th June 2015: $6.76 m SPP with $10 m Ridgeback Capital Investments LP funding: $13.8 m investment* Consolidation of CVac clinical trial program Staff reduction in FY 2015 (over 30%) Delisting from Deutsche Börse -> Trading OTC in Germany at no cost for Prim

  15. Slide 15: Outlook upcoming FY 2016

    Outlook upcoming FY 2016 • Start of AIPAC Phase IIb study with IMP321 • Start of immuno-oncology combination Phase I study • Continued development of Phase I study with IMP731 (GSK) • Start of phase I study with IMP701 (Novartis) • Potential new intellectual property • Ongoing research • Ongoing bus

  16. Slide 16: ® PRIMA BIOMED

    ® PRIMA BIOMED

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