Conference Day One | Wednesday, November 19

7:30 am Registration & Light Breakfast

8:30 am Chair’s Opening Remarks

Precision Strategies to Overcome Immune Suppression & Advance Myeloid-Targeted Therapies

9:00 am Targeting Myeloid Heterogeneity & Ferroptosis: Rethinking Suppression in Pre-Metastatic Niches

Synopsis

  • Unpack the role of myeloid cell heterogeneity in shaping immunosuppressive premetastatic environments
  • Explore ferroptosis as a regulatory mechanism of myeloid cell function and its therapeutic potential
  • Assess implications for targeting suppressive myeloid populations early to prevent metastatic progression

9:30 am Fireside Chat: Emerging Single-Target Pathways & Immune Checkpoints in Myeloid Therapy

Synopsis

  • Discover novel, single-agent targets beyond CD47 and TREM2 that are showing promise in myeloid-directed therapy
  • Examine the functional diversity of myeloid checkpoints and their role in immune suppression and resistance
  • Evaluate preclinical and translational evidence supporting these emerging targets for monotherapy or future combination strategies

10:00 am Morning Break & Speed Networking

Synopsis

As this community unites, this session will provide valuable networking time with your peers, enabling you to forge new and lasting connections.

Evaluating Advanced Models & Decoding Myeloid Heterogeneity for Improved Translational Predictability

11:00 am “Session Reserved” for GenOway

  • Kader Thiam Senior Vice President - Discovery, Preclinical Models & Services, GenOway

11:30 am Making Sense of the Myeloid Mess: Defining In Vivo Functional States & Translating them In Vitro

Synopsis

  • Explore how transcriptomic and spatial profiling datasets inform the design of advanced in vitro systems that reflect the true heterogeneity of myeloid cells across disease contexts
  • Emphasis on tools and platforms to recapitulate fibrotic environments ex vivo and allow robust readouts of myeloid cell behavior

12:00 pm Who to Treat, When to Treat? Biomarkers & Disease Stage in Myeloid Therapeutics

Synopsis

  • The importance of disease staging and how improper patient stratification can affect the efficacy of certain drugs
  • Understanding why some respond and some don’t, correlating TME features with clinical outcomes
  • Single-cell and spatial insights into late-stage vs. baseline tumors
  • Myeloid content and architecture as predictors of checkpoint response

12:30 pm Decoding Myeloid Cell State Heterogeneity in the Tumor Microenvironment to Improve Therapeutic Targeting

  • Miriam Merad Translational Research & Therapeutic Innovation, Ismms Dean, Icahn School of Medicine at Mount Sinai

Synopsis

  • Spatial, temporal, and phenotypic diversity of macrophages, neutrophils, dendritic cells
  • Understanding why immunosuppressive TAMs or neutrophils vary so much across patients
  • Highlighting the importance of longitudinal and spatial profiling to understand how heterogeneity helps shape therapy design

1:00 pm Lunch Break & Networking

Bridging the Academic Bench to Clinical Bedside Gap

2:00 pm Precision Reprogramming of Myeloid Cells to Remodel the Tumor Microenvironment

  • Nir Ben Chetrit Radiation Biology Oncology Assistant Professor, Weil Cornell Medicine

Synopsis

  • Aligning priorities: discovery science vs. commercial deliverable
  • Define shared metrics and ontologies for myeloid cell states, immune modulation, and target validation
  • Explore actionable strategies to foster alignment in priorities, communication, and clinical translational goals

2:30 pm Translating CD24, From Academic Discovery to Phase I: A Clinical Update from Pheast Therapeutics

Synopsis

  • Outline the scientific rationale and early discovery of CD24 as a novel target in myeloid-directed immunotherapy
  • Describe key preclinical validation steps and strategies used to efficiently bridge into clinical development
  • Share early clinical insights, regulatory milestones, and lessons learned from advancing CD24 into Phase I trials

3:00 pm Is Immunosuppression Really Immunosuppression & How is it Relevant to Cancer: A Novel Paradigm

Synopsis

  • The role of chronic inflammation in cancer development when immunosuppression/ immunomodulation may be useful in cancer therapy
  • The role of the retinoic acid-related orphan receptor gamma (RORy) in chronic inflammation, fibrosis and cancer
  • Targetting RORy(Immunosuppression) is not really immunosuppression but immunomodulation and is potentially beneficial in addressing the TME

3:30 pm Afternoon Break & Poster Session

Synopsis

This is your opportunity to contribute to the conversation and share your cutting-edge research with this community while discovering exciting work carried out by your peers.

Translational Strategies for Myeloid-Directed Therapies to Establish Predictive Metrics & Unify Academia, Biotech & Pharma

4:15 pm Fireside Chat: Aligning Regulatory & Funding Strategies to Accelerate Myeloid Drug Translation

Synopsis

  • What endpoints, comparators, and biomarkers regulators are prioritizing after a wave of failures in CD47, ILT, and TREM2-based programs
  • How to structure early-phase trials and IND packages to manage risk, especially for novel myeloid reprogramming or depletion strategies
  • What funders (VCs, pharma partners, government) need to see in terms of differentiation, scalability, and patient stratification to greenlight programs

5:00 pm Targeting Clever-1 in Macrophage-Driven Disease: Clinical Lessons from MDS & Beyond

Synopsis

  • MDS and AML are cancers of the macrophage lineage, in which all cancer cells express Clever-1, a master receptor of immunosuppression on macrophages
  • Targeting Clever-1 in MDS has proven extremely effective to overcome treatment resistance to standard of care agents
  • Clever-1 is found on TAMs in a number of aggressive and treatment resistant cancers and targeting Clever-1 may prove beneficial to overcome treatment resistance in a number of different cancers

5:30 pm Chair’s Closing Remarks

5:45 pm End of Conference Day One