Citeline

Dear Reader :

The IPA and Citeline wish you a prosperous New Year and hope you had a joyous, sparkling Diwali!

This month’s edition of our co-developed newsletter features an all-important discussion by global pharma chiefs on pressing issues and potential macro risks industry is faced with.

We also bring you expert opinion on the perils of over-reliance on out-licensing as a growth lever, while another piece highlights why the US FDA is keen that sponsors incorporate ‘resilience’ into clinical trials.

Anju Ghangurde - Executive Editor (Asia Pacific), Scrip/Pink Sheet
Dr. Shridhar Narayanan - Senior Technical Advisor - Innovation, IPA
IPA-Newsletter
Perspective From Industry Leaders
A Gloomy Outlook On Macro Trends From Industry CEOs FDA Offers Insights On Second Interchangeable Adalimumab
A Gloomy Outlook On Macro Trends From Industry CEOs FDA Offers Insights On Second Interchangeable Adalimumab

Pfizer CEO Albert Bourla, Eli Lilly CEO David Ricks and Seagen CEO David Epstein discussed pressing issues...

The FDA recently approved a second US Humira biosimilar, from Pfizer, as interchangeable – just a few months...

Licensing & Collaboration Agreements
Daiichi In Massive $22bn Global Deal With Merck & Co For Three ADCs How Korea Can Avoid Pitfalls Of Over-Reliance On Out-Licensing
Daiichi In Massive $22bn Global Deal With Merck & Co For Three ADCs How Korea Can Avoid Pitfalls Of Over-Reliance On Out-Licensing

The two firms will co-develop and co-commercialize three Daiichi ADCs globally outside Japan in a deal the...

An over-reliance on out-licensing as a business model may restrict the healthy growth of South Korean biopharma...

Next Gen R&D
BMS Spends $100m On Orum’s Antibody-Guided Protein Degrader Biotech Cartography: Can An AI Tool Pinpoint The Next Big Thing?
BMS Spends $100m On Orum’s Antibody-Guided Protein Degrader Biotech Cartography: Can An AI Tool Pinpoint The Next Big Thing?

ORM-6151 combines two hot approaches in cancer R&D, but clinical trials have not yet started ...

Created by Steve Lehmann, director of venture operations at Portal Innovations, Stargaze is an ...

Clinical Trials
Real-World Views On RWE: RECOVER Trial Seen As US Answer To UK’s RECOVERY ‘Resilient’ Trials: US FDA Wants To Apply COVID Lessons In Trial Design
Real-World Views On RWE: RECOVER Trial Seen As US Answer To UK’s RECOVERY ‘Resilient’ Trials: US FDA Wants To Apply COVID Lessons In Trial Design

US FDA Commissioner Robert Califf held court with global regulators to discuss the overall state of real-world....

The US FDA is not expecting sponsors to launch ‘pandemic-proof’ trials, but does want to see advance planning...

Citeline Contact

Poornachandra Tejasvi .K,
Senior Director - Emerging Markets, India
Mobile: +91 9945273146
Email: poornachandra.tejasvi@citeline.com
Client Services: clientservices@citeline.com

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IPA Contact

Name: Hari Pranav K
Email: haripranav.k@ipa-india.org