How can we work together? Partnering with Industry: An Investigator’s Perspective Robert L. Coleman, MD M. D. Anderson Cancer Center.

Slides:



Advertisements
Similar presentations
VCOM Conflict of Interest Policy Overview of Financial Conflict of Interest Related to Research December 4, 2013.
Advertisements

How to Build a Productive Relationship with NIH Topics Know your disease Know the NIH and NINDS Have realistic expectations Advocate for stronger NIH and.
Doug Elliott Professor, Critical Care Nursing Clinical research: context and importance Research Workshop: ‘Conducting research in a clinical setting’
Conflict of Interest (COI) Objectives: Provide an overview of financial conflict of interest (FCOI) related to research activities at Gillette Describe.
2nd Panel, Best Practices: “ IPR in Successful University-Industry Collaborations” Dr. Tamar Raz, CEO Hadasit, the Technology Transfer Company of Hadassah.
Conflict of Interest: Dartmouth College. Why do we care about it ? Conflict of Interest in Research : Unbiased research: design, conduct, reporting Maintain.
University of Vermont Sponsored Project Administration New PHS Financial Conflict of Interest (FCOI) Regulations Effective August 24th, 2012 Ruth Farrell,
UMBRELLA CRADAS: AN EASIER PATH AN EASIER PATH Suzanne M. Frisbie, Ph.D. Unit Supervisor Technology Transfer Center National Cancer Institute National.
ACCELERATING CLINICAL AND TRANSLATIONAL RESEARCH Anantha Shekhar MD, PhD Indiana University School of Medicine Indiana Clinical and.
NCI Designation: Expanding Science and Promoting Health in the Region Name Title, Company Date.
Research Ethics-Integrity-Governance. University Initiative:The Catalyst? ‘02 Good Research Practice Standards & Procedure to Investigate Potential Research.
Cancer Disparities Research Partnership Program Process & Outcome Evaluation Amanda Greene, PhD, MPH, RN Paul Young, MBA, MPH Natalie Stultz, MS NOVA Research.
Todays Clinical Trials. Tomorrow’s Cures. Robert L. Comis, MD 1 National Coalition for Cancer Research “Cancer 101” Congressional Briefing 09/10/14.
Translation of Anti-CD22 Monoclonal Antibodies for the Treatment of Lymphoma Joseph M. Tuscano, M.D. Associate Professor of Medicine Department of Internal.
1 The UK Opportunity: what is experimental medicine? UNLOCK YOUR GLOBAL BUSINESS POTENTIAL Pre- clinical develop- ment Phase I Phase II Phase III Product.
Research Bioethics Consultation: More potential than sequencing genomes Benjamin S. Wilfond MD Seattle Children’s Hospital Treuman Katz Center for Pediatric.
Copyright © 2013 Quintiles Quintiles Site Management Kim Davis, SSRM June 17, 2014.
Tech Launch Arizona Tech Transfer Arizona Rakhi Gibbons, Asst. Director for Biomedical and Life Sciences Licensing.
Johns Hopkins Technology Transfer 1 Translational Biomedical Research: Moving Discovery from Academic Centers to the Community Translational Biomedical.
Developing a ‘Bench to Bedside’ Commercial Collaboration Jo Chambers.
NCI Review of the Clinical Trials Process 6 th Annual National Forum on Biomedical Imaging in Oncology James H. Doroshow M.D. April 7, 2005 Bethesda, Maryland.
1 Targeted Strategies to Improve Physician and Patient Access to Cancer Clinical Research An Overview of Coalition Programs and Services Ruth Lambersky.
Compliance Issues for Medical Research at Healthcare Systems Jerry Castellano, Pharm.D., CIP Corporate Director Institutional Review Board Christiana Care.
Recognition Of Team Science Faculty Appointments, Promotions and Titles at The Geisel School of Medicine at Dartmouth “Recognition by peers as an investigator.
Indiana CTSI ACCELERATING CLINICAL AND TRANSLATIONAL RESEARCH Indiana C linical and T ranslational S ciences I nstitute Daniel F. Evans,
CONFLICTS OF INTEREST ARE HERE TO STAY: PROTECTING SCIENCE FROM BIAS Susan S. Ellenberg, Ph.D. Center for Biologics Evaluation and Research, FDA Boston,
West Virginia Clinical Translational Science Institute Links Scientists and Teachers Sara Hanks, Ann Chester, Summer Kuhn.
Margo Michaels, MPH Executive Director, ENACCT Co PI, Communities as Partners in Cancer Clinical Trials, R13-HS Panel on Use and Implementation of.
Mission: Seed, nurture, and execute large multi-disciplinary projects that involve applying computing, systems engineering, and information technology.
Activities at Academic Research Centers: Identifying Present Activities and Future Opportunities ICORD V February 24, 2009 Jim Cloyd, PharmD Lawrence Weaver.
SARC: Participation and Protocol / Concept Review Robert Maki, MD PhD Memorial Sloan-Kettering Cancer Center.
Single Patient Use of Investigational Anticancer Agents: An Industry Perspective Gerard T. Kennealey, MD Vice President, Clinical Research, Oncology AstraZeneca.
Fight On Training on NIH Conflict of Interest Rule and Introduction to diSClose Dan Shapiro Director, Research Compliance Ben Bell Manager, Research Compliance.
Partners Conflict of Interest Policy and Reporting October 11, 2012.
PUTTING THE PATIENT AT THE CENTER OF HEALTHCARE RESEARCH Towards a more inclusive model.
BioPaths-Catalyze Drug Discovery, Development and Clinical Research
National Center for Research Resources G. Iris Obrams, M.D., M.P.H., Ph.D. NCRR Update 5 August 2006.
Letters of Intent (LOIs) Through the NCI’s Cancer Therapy Evaluation Program (CTEP) Dr. Patricia M. LoRusso, D.O. Karmanos Cancer Institute Wayne State.
Challenges and healthy ageing: the role of resilience across the life course 1 st Meeting of ResNet 19 th May, 2009 Bangor University.
The Wisconsin Network for Health Research (WiNHR): Overview. An Infrastructure for Conducting Multi-Site Clinical Research across the State of Wisconsin.
Project Name Project Proposal Presentation to the Virginia Biosciences Health Research Corporation Project Management and Oversight Panel Presentation.
While most HMORN projects involve two to five Network sites, its largest consortiums are the most widely recognized. Nearly 40% of HMORN projects and consortium.
Team Building: Critical Role of Interdisciplinary Research Teams in Translational Research C. Kent Osborne, M.D. Director, Lester and Sue Smith Breast.
Initiating phase 1 clinical trials in pediatric oncology National Cancer Institute Perspective Barry Anderson, MD, PhD Pediatric Section Cancer Therapy.
The ERA-NET TRANSCAN-2, in continuity with the preceding ERA-NET TRANSCAN, aims at linking translational cancer research funding programmes in 15 Member.
MARCH 13, 2012 SERIES 2, SESSION 4 OF AAPLS NON-FEDERAL PROPOSALS: FOUNDATION AND INDUSTRY DON MCGOWAN DIRECTOR, TUFTS CFR APPLICANTS & ADMINISTRATORS.
From bench to bedside on stem cell therapy for heart repair and vice versa: do we need a new consensus? John Martin British Heart Foundation Professor.
Role of the Drug Project Team in Formulating the Initial Development Plan of NCI-IND agents Jeff Moscow, MD IDB, CTEP.
Improving the Health Literacy Environment of Wisconsin Hospitals – A Collaborative Model Sue Gaard, RN, MS Wisconsin Primary Care Research & Quality Improvement.
Why Write A Grant? Elaine M. Hylek, MD, MPH Professor of Medicine Associate Director, Education and Training Division BU CTSI Section of General Internal.
Industry’s Perspective on Industry-University Intellectual Property External Research Directors Network Industrial Research Institute, Inc. April 17, 2001.
INTANGIBLE CAPITAL AND M&A VALUE FMA - NH. Agenda Mary Adams What are IP and IC? Accounting perspective ICounting perspective Bryan Lord IP in M&A The.
Partnering With Industry for Clinical Research Luke Lin, MD, and Ralf Schnall.
1 SBIR/STTR Overview Wang Yongqiang. 2 Federal SBIR/STTR Program ‣ A +$2Billion funding program set-aside for small businesses seeking to early stage.
CTEP Visiting Physician Externship Coordinator: Igor Espinoza-Delgado, M.D. NCI CTEP Investigational Drug Branch
The TJU Human Research Protection Program (HRPP): Part I – Which Entities/Offices are Involved ? J. Bruce Smith, MD, CIP.
Mt. Hood. IOM Report: 10 Years After & More Coming Mitch Greenlick, Ph.D. Oregon State Representative April 21, 2010.
1 Impediments to Early Initiation of Pediatric Studies in a Clinical Oncology Drug Development Program A Large Pharmaceutical Company Perspective  Corporate.
Center for Biologics Evaluation and Research, FDA Site Visit Introduction Kathryn M. Carbone, M.D. Associate Director for Research.
Overcoming challenges in pediatric oncology product development: Regulatory oversight of multi-national clinical studies Ursula Kern, Advisory Committees.
Clinical and Translational Science Awards (CTSAs) Future Directions and Opportunities for ACNP investigators.
Making Clinical Trials More Efficient Site Management Organization (SMO)
Ag Ex Forum Sustainable Financial Modelling 8 th April 2016.
Research and Development Dr Julie Hankin Medical Director.
[Project Title] [Presentation Date]
[Project Title] [Presentation Date]
Universities and the Commercial World
US Early Feasibility Studies (EFS)
RECOGNITION OF CLINICAL TRIAL CANCER RESEARCH
[Project Title] [Presentation Date]
Presentation transcript:

How can we work together? Partnering with Industry: An Investigator’s Perspective Robert L. Coleman, MD M. D. Anderson Cancer Center

How can we work together? Industry Relations Spectrum: Preclinical to Phase IV The complexity of the relationship is proportional to the phase of development – Companies are organized under different management strategies to guide their pipeline (e.g. “discovery” team, late preclinical team, phase I team, “global” team) – Corporate oversight is proportional to budget Mostly collaborative but it’s important to understand the competing interests & perspectives

How can we work together? Working Well with Industry: Perspective

How can we work together? Investigator’s Goals: Perspective Oversee or participate with new therapy – Competitive advantage for site or practice Academic capital > financial (but not always) – Publications, portfolio, promotion, grants Support is linked to infrastructure costs Translational objectives: – May be “owned” by the PI’s – May be “shared” interest with Sponsor – May be “unique” to the Sponsor

How can we work together? Bench to Bedside to Bench…repeat Trials of this nature are good examples of close collaborations between industry and investigators – Examples: Home grown agents Novel therapeutics from start-ups or small research divisions in bigger companies Relatively low cost studies but relatively unlikely to result in registration paths (5% rule)

How can we work together? Competing Interests: Potential Obstacles Intellectual property Time-lines for accrual Budgets – The sense of “something for nothing…” – Drug-only trials Constrained or limited development – Combination trials with agents outside the Sponsor’s portfolio Options: CRADA or purchase – Industry may kill a potentially viable program Pemetrexed Abraxane Cast of Arrested Development

How can we work together? Competing Interests: Potential Obstacles Internal business discussions of development plans – Direction may be crafted by: Interpretation of preclinical or phase I “signals” Registration opportunities Advice from focus groups or external advisors – May be at odds with “optimal” or lengthier strategy Challenges: – Sponsor’s knowledge or understanding of the disease type/environment – Corporate way of doing things (always RP2D)

How can we work together? Challenges to Collaboration: Cooperative Groups Timelines to FPI, annual accrual, completion dates Prioritization of potentially competing agents – PARPi’s, mTOR’s, anti-angiogenics – Institutional policy against having more than 1 registration trial in the same class of agent Industry reluctance on registration paths (FDA or EMEA package) Reluctance of the cooperative groups to participate with industry if they feel the data is not or cannot be independently auditable Costs associated with translational objectives Important to have a “champion” who can tactfully navigate the bureaucracy

How can we work together? Challenges to Collaboration

How can we work together? Challenges to Collaboration COI: industry relationships are being increasingly scrutinized in clinical investigation – Many of the most experienced Investigators are necessarily “tapped” for advice in development Investigator (NCI) definition: – “’Investigator’ means the Principal Investigator AND any other person who is responsible for the design, conduct, or reporting of research funded by PHS, or proposed for such funding.” “…relating to financial interests, ‘Investigator’ includes the Investigator’s spouse and dependent children” Significant COI requires reassignment of the Investigator, consent disclosure, and transfer of patient care while on study

How can we work together? Building Industry Rapport Strong relationships can lead to important and expeditious milestones in clinical medicine Important to understand the issues upon which industry and the scientific community wrestle to optimize collaborative interaction Communication, confidence and transparency are key to this process

How can we work together? Thanks!