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Business & Regulation Trends & Forecasts

Drugs to Watch in 2025: Part 2

| Stephanie Vine | 9 min read

We take a deep dive into key industry trends off the back of Clarivate’s Drugs to Watch 2025 report

Business & Regulation Business Practice

Biden’s Legacy; Trump’s Agenda: Part 2

| 7 min read

In part 2 of our roundtable discussion, thought leaders discuss what Trump could do for drug pricing and whether change is to be feared or embraced.

Business & Regulation Trends & Forecasts

Drugs to Watch in 2025: Part 1

| Stephanie Vine | 8 min read

We speak with Clarivate about their report listing eleven key drugs to watch in 2025.

Discovery & Development Clinical Trials

Asking the Right Questions in R&D

| 3 min read

And getting the right people involved from the start. Here’s why collaboration is key for successful clinical development.

Discovery & Development Drug Delivery

The Force Meets Oligonucleotides

| Stephanie Vine

Researchers develop a new platform to improve delivery of oligonucleotide therapies to muscle.

Business & Regulation Business Practice

Biden’s Legacy; Trump’s Agenda: Part 1

| 10 min read

Biden pushed drug pricing reforms, whereas Trump is known for deregulation. What does this mean for pharma?

Business & Regulation Supply Chain

The UK's Radiopharma Revolution

| Juliana Maynard | 6 min read

Radiopharmaceuticals are a promising approach to cancer, but some countries are lagging behind. A collaboration hopes to change that.

Discovery & Development Drug Discovery

Rethinking Osteoarthritis With Extracellular Vesicles

| 4 min read

Why researchers are excited about the potential of extracellular vesicles from umbilical cord-derived stem cells.

Discovery & Development Drug Discovery

Breaking Through Rare Diseases

| Stephanie Vine | 8 min read

We asked three rare disease drug developers about their work, the challenges facing the field, and what they would do with unlimited funds.

Discovery & Development Drug Delivery

RIDE: A New Approach to CRISPR Delivery

| Rob Coker | 2 min read

A new study reports targeted CRISPR delivery in retinal and neurological disease models – without viral vectors.

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