Research Field


Research Field Drug discovery

Biologically Driven

| 4 min read

Academia has its appeal for many; for others the real challenges are in industry. Here, IO Biotech CEO Mai-Britt Zocca discusses her own motivations.

Research Field Drug discovery

Release the Beast

| Pandora Pound | 5 min read

The FDA Modernization Act opens the door for more innovative alternatives to animal testing for drug discovery and development

Research Field Drug discovery

Opiate Dreams and Nightmares

| Jamie Irvine | 3 min read

Experimental insomnia drug shows promise in alleviating opioid withdrawal symptoms and opioid-seeking behavior

Research Field Drug discovery

Minds, Interrupted

| Alex Fornito, Ashlea Segal | 2 min read

Researchers develop a new approach to mapping the individual heterogeneity of brain changes in mental disorders

Research Field Drug discovery

Alzheimer’s Disease: The Winds of Progress

| Jamie Irvine | 10 min read

Howard Fillit shares his views on the historical research lag, the slim successes so far, and the target pathways that offer most hope

Research Field Drug discovery

The PEPITEM Pathway – and the Path to New Obesity Treatments

| Stephanie Vine | 6 min read

The world needs new medicines to treat obesity-related conditions. Here’s what researchers at the UK’s University of Birmingham are doing about it.

Research Field Drug discovery

Honey, I Shrunk the Molecules

| Jamie Irvine | 2 min read

Researchers demonstrate that microRNA-132 can significantly affect different brain cells, with potential implications for Alzheimer’s disease.

Research Field Drug discovery

Addressing Alzheimer’s

| 3 min read

The more we learn about the complexity of Alzheimer’s, the more we need to change the way we treat it

Research Field Drug discovery

Lonely Hearts Club

| Jamie Irvine | 4 min read

TUM Researchers create organoid that emulates the development of the human heart

Research Field Drug discovery

Big Problem, Mini Solution

| Jamie Irvine | 6 min read

Researchers have designed a “mini gene” therapy that could hold promise for treating Usher Syndrome Type 1F


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