Bio-Path Holdings, Inc. · OTC:BPTH

Bio-Path — Investor Presentation (May 2022)

12 slides from Bio-Path's investor presentation, May 2022

  1. Slide 1: Bio-Path Holdings: An Oncology-Focused Biotechnology Company

    Bio-Path Holdings An Oncology-Focused Biotechnology Company May 2022

  2. Slide 2: Forward looking statements

    Forward looking statements This Presentation contains forward-looking statements with respect to business conducted by Bio-Path Holdings, Inc. By their nature, forward-looking statements and forecasts involve risks and uncertainties because they relate to events and depend on circumstances that will

  3. Slide 3: Introducing Bio-Path Holdings

    Introducing Bio-Path Holdings Advanced Oligonucleotide Therapeutics with High Efficiency Systemic Delivery Publicly traded Employees, Established NASDAQ Contractors & Houston, TX Consultants BPTH 2007 14 Technology Highlights ® DNAbilize Technology, next generation single-stranded DNA antisense Robu

  4. Slide 4: Robust Oncology Pipeline

    Robust Oncology Pipeline Preclinical IND PHASE 1 PHASE 2 Prexigebersen (BP1001, Liposomal Grb2) AML* *Orphan drug designation from the USFDA and BP1001-A Solid Tumors (ovarian, endometrial, EMA for AML pancreatic) BP1002 (Liposomal Bcl-2) Lymphoma, CLL BP1002 (Liposomal Bcl-2) AML venetoclax failure

  5. Slide 5: DNAbilize Technology

    DNAbilize Technology ® Proven As Safe, Robust and Targeted Method for Treating Disease No Toxicity No Toxicity With human patients to date in prexigebersen clinical trial. • DNAbilize™ liposome structure is similar to the cellular membrane • P-ethoxy DNA does not induce hepatotoxicity or thrombocyto

  6. Slide 6: Stage 1 of the Phase 2 Efficacy Trial Design for AML Prexigebersen Combination Therapy

    Stage 1 of the Phase 2 Efficacy Trial Design for AML Prexigebersen Combination Therapy • Treatment of untreated AML patients who are induction therapy ineligible and unfit for stem cell transplant • Efficacy trial conducted at 6 leading cancer centers in the U.S., including the MD Anderson Cancer Ce

  7. Slide 7: Data from Ongoing Phase 2 Study of Prexigebersen at 2021 ASH Annual Meeting

    Data from Ongoing Phase 2 Study of Prexigebersen at 2021 American Society of Hematology Annual Meeting  Prexigebersen Data Show Signs of Safety and Efficacy in High Risk AML Patients  In the Poster we report the safety run-in and efficacy data of AML patients treated with prexigebersen + decitabin

  8. Slide 8: Experienced Leadership Team

    Experienced Leadership Team Officer and Director Peter Nielsen since founding Michael Hickey 20+ years experience across all phases of drug Co-Founder, President, Company in 2007 Director Clinical development Chief Executive Officer Program Management and Chief Financial Manufacturing Officer Point

  9. Slide 9: Scientific Advisory Board

    Scientific Advisory Board Jorge Cortes, M.D. • Director, Cancer Center at Augusta University • Georgia Research Alliance Eminent Scholar in Cancer Chairman • Formerly, Jane and John Justin Distinguished Chair in Leukemia Research, Chief of the AML and CML sections, and Deputy Chair of the Department

  10. Slide 10: IP and Financial Snapshot

    IP and Financial Snapshot Intellectual Property • Original patents licensed from MD Anderson • New composition and methods of use patent issued covers DNAbilize® technology, solely owned by Bio-Path • Five patents issued in the U.S.; two foreign patents issued • Six additional applications pending i

  11. Slide 11: Accomplishments in 2021

    Accomplishments in 2021  We presented a poster at the 2021 American Association for Cancer Research (AACR) Annual Meeting in April that summarized preclinical studies that demonstrated the effectiveness of BP1002 + decitabine combination treatment in venetoclax resistant cells opening potential new

  12. Slide 12: Thank you

    Bio-Path Holdings Thank you Bio-Path Holdings, Inc. 4710 Bellaire Blvd Suite 210 Bellaire, TX 77401 Web: www.biopathholdings.com Mail: partnering@biopathholdings.com Tel: (832) 742-1369 12

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