Crescent Biopharma, Inc. · NASDAQ:CBIO

Crescent Biopharma — Glycomimetics — Merger or Acquisition (February 2025)

27 slides from Crescent Biopharma's merger presentation, Feb 28, 2025

  1. Slide 1: Crescent Biopharma Overview

    March 2025 Crescent Biopharma Overview ​ ​ ​ ​

  2. Slide 2: Disclaimers

    2 Disclaimers This presentation is for informational purposes only and only a summary of certain information related to Crescent Biopharma, Inc . (“we”, “Crescent” or the “Company”) . It does not purport to be complete and does not contain all information that an investor may need to consider in mak

  3. Slide 3: Crescent Biopharma aims to advance the next wave of innovation in cancer therapy

    3 Crescent Biopharma aims to advance the next wave of innovation in cancer therapy 1. Anticipated expiration for filed provisional patent is 2045+ 2. Financing scheduled to close immediately prior to the closing of the merger with GlycoMimetics Notes: NSCLC: Non - small cell lung cancer. MoA : Mecha

  4. Slide 4: Three oncology programs with best-in-class potential

    4 Crescent is advancing three highly impactful oncology programs with best - in - class potential Notes: bsAb : Bispecific antibody. IND: Investigational New Drug application. PoC: Proof - of - concept CR - 001 PD - 1 x VEGF cooperative tetravalent bsAb Same MoA as ivonescimab Designed to reproduce

  5. Slide 5: Multiple ways to win: pipeline enables optionality with combination therapies

    5 Multiple ways to win: Crescent pipeline enables optionality with differentiating combination therapies Optimized Novel Monotherapies Synergistic Combination Approaches CR - 001 CR - 002 CR - 003 CR - 001 + CR - 002 CR - 001 + CR - 003 Engineered for: Best - in - class efficacy Efficacy across hist

  6. Slide 6: Three key advances in oncology for next-generation combinations

    6 Crescent leverages three key advances in oncology for next - generation combinations within unique portfolio EVOLUTION OF CHEMOTHERAPY Enhanced efficacy & safety via cooperativity Enhanced efficacy & safety via targeting ADC PD - (L)1 Cooperative bispecific PD - 1 x VEGF Systemic chemo CR - 002 CR

  7. Slide 7: PD-(L)1-targeted therapies have transformed oncology

    7 PD - (L)1 - targeted therapies, annualizing $50B+, have transformed oncology – with Keytruda now the best - selling drug in the world 1. 5 - year follow - up demonstrated mOS of 22.0 vs 10.6 months. 2. Notes: 1L: First - line. NSQ: Non - squamous. NSCLC: Non - small cell lung cancer. mOS : median

  8. Slide 8: Ivonescimab doubled progression-free survival vs. Keytruda in a P3 NSCLC trial

    8 Ivonescimab, a cooperative PD - 1 x VEGF bispecific, doubled progression - free survival vs. Keytruda in a P3 NSCLC trial Notes: HR: hazard ratio. PFS: progression - free survival. AE: adverse event. NSQ: Non - squamous SQ: Squamous. ORR: Objective response rat e. Akeso Biopharma has licensed ivon

  9. Slide 9: Cooperative, tetravalent PD-1 x VEGF bispecific antibody

    9 CR - 001 Cooperative, tetravalent PD - 1 x VEGF bispecific antibody ​ ​ ​ ​

  10. Slide 10: Ivonescimab's novel, cooperative MoA

    10 Ivonescimab’s novel, cooperative MoA is hypothesized to drive enhanced anti - tumor activity while maintaining tolerability Sources: 2023 Zhong (SITC Poster); Summit Therapeutics VEGF drives tumor angiogenesis PD - L1 expression suppresses T cells Tumor Microenvironment (TME) VEGF PD - L1 PD - 1

  11. Slide 11: Highly potent PD-1 x VEGF bsAb designed to recapitulate ivonescimab's pharmacology

    11 CR - 001 is a highly potent PD - 1 x VEGF bsAb designed to recapitulate ivonescimab’s cooperative pharmacology Notes: IgG: Immunoglobulin G. scFvs : S ingle - chain variable fragment. ADCC: A ntibody - dependent cell - mediated cytotoxicity; PK: Pharmacokinetics. FcRn: N eonatal Fc receptor. CR -

  12. Slide 12: Replicates ivonescimab's cooperative binding effect

    12 CR - 001 replicates ivonescimab’s cooperative binding effect which leads to cooperative inhibition of PD - 1 signaling in presence of VEGF Notes: Ivonescimab generated internally based on published sequence. PD - 1 / PD - L1 signaling inhibition measured in RLU (relative light units), a measure o

  13. Slide 13: Engineering replicates ivonescimab function with biophysical properties

    13 CR - 001 engineering replicates ivonescimab function with biophysical properties that maximize flexibility in development Notes: CDR: Complementarity - determining region. CDC: Complement - dependent cytotoxicity. Fc: Fragment crystallizable. Ivonescimab’s unique structure and geometry – and resu

  14. Slide 14: Potential to transform standard of care across oncology indications

    14 CR - 001 has potential to transform SoC across a multitude of oncology indications, with numerous first - in - class opportunities Notes: EGFRm = mutant epidermal growth factor receptor. Sources: Keytruda Label; Opdivo Label; Tecentriq Label; Imfinzi Label; Libtayo Label; Bavencio Label; Jemperli

  15. Slide 15: Late-stage competitor programs with P3 PFS and OS readouts

    15 Development programs across key late - stage competitors include numerous P3s with PFS & OS readouts, paving the way for CR - 001 Notes: List of trials not exhaustive; BNT327 - 06 is a master protocol for two P2/3 sub - studies; BNT327 P2/3 in NSCLC announced Nov 2024 but details not yet availabl

  16. Slide 16: Two parallel development paths

    16 TWO PARALLEL DEVELOPMENT PATHS FOR CR - 001 Parallel clinical development paths offer potential for both first - in - class and lower risk opportunities for CR - 001 First - in - class opportunities Numerous indications with clinically meaningful anti - PD - (L)1 +/ - VEGF efficacy and potential

  17. Slide 17: Phase 1 data offer potential for early acceleration

    17 CR - 001 Phase 1 data offer potential for early acceleration – a rarity for a solid tumor oncology program High conviction in CR - 001’s clinical profile can be reached in ~9 - 12 months from Phase 1 initiation, offering potential for significant early value inflection Phase 1 interim proof - of

  18. Slide 18: Only five known constructs with ivonescimab-like cooperative pharmacology

    18 Only five known constructs with potential to exhibit ivonescimab - like cooperative pharmacology Sources: Internal data; Summit Therapeutics 2023 SITC Poster; Compass Therapeutics Jan 2025 Corporate Presentation and press release; Bio NTech 2024 ESMO Presentation; LaNova patent filings; Various p

  19. Slide 19: Preclinical data reproduce ivonescimab's breakthrough pharmacology

    19 CR - 001 preclinical data reproduce ivonescimab’s breakthrough pharmacology & are rapidly advancing to generate significant value Unprecedented third - party data validate PD - 1 x VEGF cooperativity Transformative MoA for $50B+ market CR - 001’s proprietary engineering is designed to replicate i

  20. Slide 20: CR-002 & CR-003: Topoisomerase inhibitor ADCs against validated targets

    20 CR - 002 & CR - 003 Topoisomerase inhibitor ADCs against validated targets ​ ​ ​ ​

  21. Slide 21: CR-002 and CR-003 are potentially best-in-class topoisomerase inhibitor ADCs

    21 CR - 002 and CR - 003 are potentially best - in - class topoisomerase inhibitor ADCs, with applicability across solid tumors Potential to synergize with CR - 001 and other immunotherapies Each ADC can be leveraged in combination studies in solid tumors Validated, undisclosed solid tumor ADC targe

  22. Slide 22: ADCs with topoisomerase inhibitor payloads show best-in-modality efficacy and safety

    22 ADCs with topoisomerase inhibitor payloads have demonstrated best - in - modality efficacy and safety Notes: GEJ: Gastroesophageal junction. A: Approved. R: In registration. PN rates are weighted averages, by number of patients, acros s i ndications / trials and include PN, PSN, PMN, and PSMN whe

  23. Slide 23: Corporate

    23 Corporate ​ ​ ​ ​

  24. Slide 24: Executive Team and Board of Directors

    24 Executive Team Jonathan Violin, PhD Interim CEO Chris Doughty Chief Business Officer Barbara Bispham General Counsel Ryan Lynch Chief Accounting Officer Jonathan Violin, PhD Alex Balcom Susan Moran, MD Peter Harwin Board of Directors Rapidly growing leadership team with deep experience building t

  25. Slide 25: Financing expected to fund programs through key value-generating catalysts

    25 Financing expected to fund Crescent programs through key anticipated value - generating catalysts Notes: mNSCLC : Metastatic non - small cell lung cancer. ES: Extensive stage. EGFRm: Mutant EGFR. Sources: ClinicalTrials.gov ; Company websites 2025 2026 Current cash expected to fund operations thr

  26. Slide 26: Estimated capitalization following close of transactions

    26 Estimated capitalization following close of transactions Pre - closing financing Shares of common stock outstanding Shares of common stock outstanding Shares of common stock Pre - funded warrants Series A shares 64,532,953 105,137,814 298,298,000 1,339,680,730 273,643,080 Estimated total shares o

  27. Slide 27: Thank you

    Thank you ​ ​ ​ Forward-Looking Statements This communication contains forward-looking statements (including within the meaning of Section 21E of the Exchange Act and Section 27A of the Securities Act) concerning GlycoMimetics, Crescent, the proposed transactions and other matters. These forward-loo

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