Out of order: I am not an animal

Companies may need to share preclinical data with investors, the trade press and the like, but perhaps sharing a lot less of that early-stage data with the general public would be a good idea
| 3 min read
Register for free to listen to this article
Listen with Speechify
0:00
3:00
At a pivotal moment in the movie “The Elephant Man,” John Merrick is chased through the streets by a mob of men in top hats. As they corner him in a public restroom, he finally cries out: “I am not an animal. I am a human being.”
Continue reading below...
A black mosquito is shown on pink human skin against a blurred green backdrop.
InfographicsDiscovering deeper insights into malaria research
Malaria continues to drive urgent research worldwide, with new therapies and tools emerging to combat the parasite’s complex lifecycle and global burden.
Read More
During an interview for last month’s Special Report on Stem Cells, Calimmune CEO Louis Breton recounted his company’s efforts at gene therapy for the treatment of HIV. At one point, he made a statement that I hear time and again in these interviews: “We tested that in animals with great results, but as everybody knows, animals are not humans.” (Note: The treatment is in Phase 1/2 studies.)
Last week—and this will be true no matter when you read this—a news item described amazing results by scientists to treat a disease, giving hope that the debilitating condition might soon become a thing of the past.
I know this, because like probably all DDNews readers, I had to explain to friends and family why the promise might be a bit overstated, if only because the study was done on lab animals, and well, you know.
Which brings me to my point: Why do we even bother to issue press releases about findings in animals?
Continue reading below...
A white, pink, and blue 3D molecular structure of a simple sugar is shown against a light purple background.
WebinarsAdding a little sugar: what glycomics can bring to medicine
Discover how glycoscience is transforming how scientists understand diseases and opening new doors for drug discovery.
Read More
In-vitro and animal models of disease are vital steps in the understanding of pathology and the discovery of therapies, let there be no doubt. It would be unconscionable to introduce a therapeutic to a human subject without feeling we had discovered all we could about its safety and efficacy.
But we also recognize that these models are just that: models. Despite our best attempts to make them as representative as possible, they are flawed. But then, so are clinical trials.
It is the nature of scientific enquiry to be flawed, if only because we don’t already know everything. If we did, you’d now be reading my commentary on actuarial tables or some other subject because we’d all be working in a different field.
But where we have the training and experience to understand this, to read scientific studies and interpret conference talks and posters with respectful grains of salt, my mom doesn’t. She is more apt to get excited by the results of the latest study into a disease germane to her world, not necessarily realizing that it was done in worms or sheep or knowing why that matters.
Continue reading below...
An illustration of various colored microbes, including bacteria and viruses
WebinarsCombatting multidrug-resistant bacterial infections
Organic molecules with novel biological properties offer new ways to eliminate multidrug-resistant bacteria.
Read More
Instead, she excitedly posts a link on Facebook.
As the people doing the research, I completely understand the desire to share your work with others and to have people appreciate the importance of the stepping stone you have provided to the conversation. Trust me, I understand. My Master’s degree involved bacteriophage lambda, an organism that now largely resides in the backwater of biology.
And as the universities, government agencies and companies that rely on outside investment to continue your work, I get the need to keep people apprised of your progress, if only to ensure a continued influx of monies from donors, taxpayers or shareholders.
But how often can we cry preclinical victory and later disappoint people when the promises don’t survive the clinical jump before people stop believing us and, more importantly, in Science (the pursuit, not the journal)?
Already, the developed world is filled with non-believers who point at conflicting studies or highlight one failed drug after another as evidence that the system is rigged or that scientists haven’t a clue what is happening.
Continue reading below...
A syringe with a needle drawing the vaccine out of a vial with ampules in the background
InfographicsTurbocharging mRNA vaccine development
Cell-free gene synthesis technology offers a quick, reliable route to creating vital mRNA vaccines and therapeutics.
Read More
Sure, the media can take some of the blame here.
Despite the efforts of incredibly good science and medicine journalists, most writers and editors want the hot and sexy angle of a story. We all do. And what that translates to is readers not learning that the study was performed on mice until the last few paragraphs, if at all.
So fine, it is an education issue with journalists. But while we are teaching them the finer points of scientific enquiry and cautious optimism, can we not stop feeding the beast with hopeful allusion, excited overstatement and outright hyperbole?
Publish your scientific papers. Announce your findings at conferences. Share your thoughts and experiences with the trade press (e.g., DDNews). Populate your annual reports with status updates.
But until we have concrete clinical trial results with contextual analysis, let’s stop including my mom and her friends into the conversation. They get too excited at the announcements and depressed by the recalls.

About the Author

Related Topics

Published In

Loading Next Article...
Loading Next Article...
Subscribe to Newsletter

Subscribe to our eNewsletters

Stay connected with all of the latest from Drug Discovery News.

Subscribe

Sponsored

Fluorescent-style illustration of spherical embryonic stem cells clustered together against a dark background.
Explore how emerging in vitro systems — built from primary cells, cocultures, and vascularized tissues — are improving translational research outcomes. 
3D illustration of ciliated cells, with cilia shown in blue.
Ultraprecise proteomic analysis reveals new insights into the molecular machinery of cilia.
3D illustration showing a DNA double helix encapsulated in a transparent capsule, surrounded by abstract white and orange protein-like molecular structures against a blue background.
Discover an integrated analytical approach that unites identification, purification, and stability assessment for therapeutic molecules.
Drug Discovery News December 2025 Issue
Latest IssueVolume 21 • Issue 4 • December 2025

December 2025

December 2025 Issue

Explore this issue