Explore the Agenda

7:00 am Doors Open for Registration, & Pre-Event Networking

7:50 am Organizer Opening Remarks

Opportunities & Deal Trends Following Best-in-Class Opportunity in Oncology

8:00 am Pharma Icebreaker Panel Discussion: Targeted Oncology Biologics

Former - Chief Executive Officer, CrossBridge Bio
Director, Oncology Search & Evaluation, Business Development & Licensing, Merck & Co
Senior Director, Oncology Business Development, AstraZeneca
Vice President, Head of Oncology Search & Evaluation, Ipsen Pharma
Executive Director, Johnson & Johnson
Associate Director, Oncology Search & Evaluation, Takeda Pharmaceutical
Director of S&E, Novartis AG
Scouting and Transaction Lead, Astellas Pharma
Global Director, Research & Technology Search & Evaluation, Daiichi Sankyo
  • Understanding what it takes for pharma to invest. What are the current budgetary considerations within pharma?
  • How is pharma assessing novel technologies, and where do they place within portfolios?
  • What feels differentiated in a crowded space? From pharma’s perspective, what will make something best-in-class?

Conviction to Transact in Immunology: Data or FOMO?

8:40 am Pharma Icebreaker Panel Discussion: Investing into Immune Rest, Rebalance & Reconstitution

Director, Strategic Partnering (Immunology), Global BD&L, Boehringer Ingelheim
Head of Search and Evaluation- Respiratory and Immunology, AstraZeneca
Senior Director, Immunology Therapeutic Area Lead, Johnson & Johnson
Executive Director BD&L, Infectious Disease, Vaccines, Oncology, Merck & Co
Search & Evaluation Lead, GI & Inflammation, Strategy & Portfolio Development, Takeda Pharmaceutical
Director - Strategic Research & Development, Otsuka America Pharmaceutical, Inc
Chief Business Officer, Foghorn Therapeutics
Director, Search and Evaluation Immunology, Sanofi
  • Which stage of development is most appealing in Immunology?
  • What are the starting points, from a data package perspective, when it comes to assessing engagers or in vivo CAR-T?
  • When evaluating an early-stage what level of data—whether safety, biomarkers, or efficacy—provides you with conviction that the program has true drug potential?
  • Which diseases do you think are most promising for B-cell targeted therapies?

9:20 am Short Comfort Break to Arrange Organized Networking Session

9:30 am Pharma Icebreaker Tables: Accelerating Connections

  • The pharma icebreaker tables running in each track create introductions between biotech and pharma
  • Two weeks out from the conference, pharma will review attending biotech and biotech will review attending pharma, with both making selection to meet with companies they haven’t scheduled meetings with yet through the One-to-One Partnering Portal
  • With these selections, we will build a schedule of company rotations through each pharma’s table
  • Join three tables, led by three pharma, for 30 minutes each. Mixed groups rather than 1-2-1s, hear how your peers pitch themselves whilst also getting facetime with pharma yourself, first thing on day one

11:15 am Morning Break & One-to-One Partnering Meetings Open for Day One

In vivo CAR-T versus TCEs: Where Does the Future Land?

11:45 am Scientific, Operational & Economic Realities for Immune-Modulating Therapies: What Have we Learnt so Far?

Senior Director, UCB
Executive Director - Venture Fund, Boehringer Ingelheim
Chief Executive Officer, Liberate Bio
Head of Oncology Research & Development, Sana Biotechnology
Founder & Chief Executive Officer, Kali Therapeutics
  • Pharma’s reflections on recent in vivo CAR-T and TCE deals, what data was valuable when clinical data was minimal?
  • Overlapping and diverging advantages of TCEs to in vivo CAR-T, including depth and durability of response.
  • Debating clinical-adjacent innovations in delivery across viral vectors and LNPs and their application in immunology versus oncology

Is on-Target Toxicity a Bad Thing? The Balance Between Efficacy & Worsening Toxicity

12:15 pm Tumor Selectivity Strategies Across Multispecifics, TCEs, & ADCs: What Have we Learnt so Far?

Head of Large Molecule & ADC Innovation, Eli Lilly & Co.
Head of Corporate Development, DCx Bio
Chief Executive Officer & Co-Founder, Voro Therapeutics
Founder & Chief Executive Officer, VelaVigo
Co-Founder & Chief Executive Officer, Valink Therapeutics
Chief Scientific Officer, Zymeworks
  • Engineering conditional activation through masking and pre-dosing in TCEs and ADCs
  • Discussing dual-target and multispecific approaches
  • Applying induced proximity to ADC specificity to substantially change the behaviour of an ADC

12:45 pm Lunch Break & Networking Opportunity

Where do DACs fit in 2026/27 Portfolios? From Preclinical Promise to First-in-Human

2:00 pm Increasing the Therapeutic Index of a Small Molecule as Precision ADCs: What Have we Learnt so Far?

Chief Scientific Officer, Cullgen Inc.
Senior Vice President, Business Development, Orum Therapeutics, Inc.
President & Chief Executive Officer, Fortitude Biomedicines
Chief Business Officer, Nurix Therapeutics, Inc.
  • Designing DACs to be a more targeted to oncogenic drivers versus traditional small molecule inhibitors
  • Discussing initial proof-of-concept case studies for DACs
  • Collaboration potential between antibody engineering and protein degradation companies

2:30 pm Presentation Session One: Showcase Your Science

Head of Large Molecule & ADC Innovation, Eli Lilly & Co.

Present your company’s slides by securing a 15-minute presentation slot in front of the

attending audience.

What is this session?

At the intersection of innovative research and business conversations, this forum facilitates the

pitching of biotech pipelines and platforms to attending pharma and investors.

How does this session work?

As you register, secure one of the 15-minute presentation slots available in this presentation

session and position your differentiation as part of the conference line-up. We will add your

talk to this brochure and on our website to showcase your differentiation in the best light and

share your corporate summary with all attendees as part of pre- and post-event content, to drive

interest and follow-up in your session.

Who can present?

Those developing in-house pipeline or platform technology, without any additional service

provider capabilities, such as contract research or manufacturing.

2.00 Presentation by SKYMAB Biotherapeutics

2.15 Presentation by Bicycle Therapeutics

2.30 Presentation by Rapafusyn

3:30 pm Afternoon Break & One-to-One Partnering Meetings Restart

4:15 pm 2025/26 Deal-Making Highlights: How Did They Happen?

Chief Executive Officer, JEO Biotech Advisors
Head of BD&L USA & Global TA Inflammation, Boehringer Ingelheim
Head of Large Molecule & ADC Innovation, Eli Lilly & Co.
Former - Chief Executive Officer, CrossBridge Bio
President, Chief Operating & Business Officer, Epimab Biotherapeutics
Senior VP, Strategic Alliances & Business Development, C4 Therapeutics
Chief Business Development Officer, Immunai
  • Representing examples of successful deal-making and successful management of alliances to foster future deals, what are the learnings?
  • Sharing how early-stage programs can successfully navigate the “show me data” barrier with pharma, and the activation barrier to licencing technologies between equal sized biotech
  • Debating recent regulatory and emerging technology shifts, and how these will shape licensing deals for the discussed modalities

5:00 pm Drinks Reception

Connect more casually at the end of day one drinks reception. Enjoy an informal networking with all attending colleagues, to follow up with contacts from other partnering initiatives, catch those you haven’t already run into, and meet with old connections again in-person. Deliberately timed ahead of key events in the business development calendar, use this as an opportunity to become front-of-mind, and start conversations going into the Fall calendar.