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12 Questions with Jackie Marchington

Jackie Marchington is Head of Compliance and Ethics for IPG Health Medical Communications.

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Seeking effective, safe treatment for all with precision dos...

Modern medicine moves ever more to precision, personalised medicine, and precision dosing is critical in a world that recognises biological individuality – especially when it comes to paedi

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Gilead looks beyond Trodelvy with Tubulis alliance

Gilead Sciences has shored up its antibody-drug conjugate pipeline by licensing a candidate from German biotech Tubulis in a deal worth up to $415m.

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Cytokinetics' president and chief executive Robert Blum

FDA kicks off review of Cytokinetics' aficamten for HCM

Cytokinetics should hear back from the FDA next September about its application for Camzyos rival aficamten in obstructive hypertrophic cardiomyopathy

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Ipsen doubles up in TCEs for cancer, adding Biomunex drug

Ipsen has expanded its oncology pipeline by licensing a T cell engager (TCE) therapy from Paris-based startup Biomunex for up to $610m.

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Seeking effective, safe treatment for all with precision dos...

Modern medicine moves ever more to precision, personalised medicine, and precision dosing is critical in a world that recognises biological individuality – especially when it comes to paedi

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Deep Dive: Patients & Partnerships 2024

IN THIS ISSUE: The 2024 US Presidential race is nearing its end, but what does that mean for pharma?

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The AI effect in pharma commercial strategy: From data to re...

Discover how AI is transforming the pharma commercial strategy. Unlock real-time insights & actions from data. Click here for more.

Digital

Seeking effective, safe treatment for all with precision dos...

Modern medicine moves ever more to precision, personalised medicine, and precision dosing is critical in a world that recognises biological individuality – especially when it comes to paedi

Market Access

Lori Fletcher and Amber Beimer, Advanced Clinical

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Health Innovators: Lori Fletcher and Amber Beimer, Advanced ...

Clinical research is full of challenges, from recruitment to data management to global resourcing.

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How to deal with fragmented data - A $12.9 million challenge

In the age of AI, large data sets – like the treasure trove of customer data most biopharma companies are sitting on – are an invaluable asset.

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Gilead looks beyond Trodelvy with Tubulis alliance

Gilead Sciences has shored up its antibody-drug conjugate pipeline by licensing a candidate from German biotech Tubulis in a deal worth up to $415m.

News

FDA kicks off review of Cytokinetics' aficamten for HCM

Cytokinetics should hear back from the FDA next September about its application for Camzyos rival aficamten in obstructive hypertrophic cardiomyopathy

News

Ipsen doubles up in TCEs for cancer, adding Biomunex drug

Ipsen has expanded its oncology pipeline by licensing a T cell engager (TCE) therapy from Paris-based startup Biomunex for up to $610m.

News

'UK Only' red stamp on manufacturing facility

Deadline looms for post-Brexit label changes for UK meds

The MHRA has reminded pharma companies that from 1st January all medicines sold in the UK will have to comply with new labelling requirements.

Views & Analysis

Digital

Seeking effective, safe treatment for all with precision dos...

Modern medicine moves ever more to precision, personalised medicine, and precision dosing is critical in a world that recognises biological individuality – especially when it comes to paedi

Sales & Marketing

Sponsored

12 Questions with Jackie Marchington

Jackie Marchington is Head of Compliance and Ethics for IPG Health Medical Communications.

Market Access

Part Two: Navigating the complexities of global market acces...

The journey to global market access for innovative therapies is fraught with challenges that vary significantly across the world.

Market Access

Part One: Overcoming challenges and seizing opportunities in...

The outlook for drug development to treat rare diseases looks encouraging, offering hope to the 300 million people globally facing the significant challenges of these often-overlooked condi

Deep Dive

Patients

Pills and polls: What the 2024 election means for pharma

Patients

Empathy in action: Designing person-focused healthcare mater...

Patients

Beyond clinical trials: Unleashing the power of patient-repo...

Patients

Advancing patient care through early and sustained collabora...

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Sponsored

The AI effect in pharma commercial strategy: From data to re...

Discover how AI is transforming the pharma commercial strategy. Unlock real-time insights & actions from data. Click here for more.

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Enabling site success: Key insights to reducing burden and i...

Investigator sites are essential for successful execution of clinical trials – ensuring studies are conducted ethically, safely, and in compliance with regulatory standards.

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HCP holding tablet with AI visual applied

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Decoding physician prescribing behaviour: A data-driven jour...

Identifying high-volume prescribers and engaging with key opinion leaders (KOLs) in a target therapeutic area can be a challenge.

R&D

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Beyond clinical: Boosting recruitment and retention with SDO...

The success of clinical trials hinges on a complex array of factors, many of which extend beyond traditional clinical care.

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Digital

Seeking effective, safe treatment for all with precision dos...

Modern medicine moves ever more to precision, personalised medicine, and precision dosing is critical in a world that recognises biological individuality – especially when it comes to paedi

Oncology

CAR-T therapies: Faster, better, cheaper

In a new pharmaphorum podcast, editor-in-chief Jonah Comstock speaks with Phil Johnson, MD, president and CEO of Interius Biotherapeutics.

Market Access

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Health Innovators: Lori Fletcher and Amber Beimer, Advanced ...

Clinical research is full of challenges, from recruitment to data management to global resourcing.

Market Access

Looking to history to prepare for America’s uncertain future

In this podcast episode, Jesse Mendelsohn and Nicole Raleigh discuss what the future might hold for pharma under a second Trump Administration

Significant breakthroughs in CNS biology, coupled with innovative neuroscience technologies and a more supportive regulatory landscape, have fuelled increased investment and pharmaceutical interest

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