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The questions that take an hour elsewhere, answered in one click.

TheraRadar is a competitive intelligence platform for pharma and biotech. Search any drug, company, or target and get the answer with the live data behind it.

Latest from TheraRadar Briefs

Long-form pharma intelligence, published weekly on TheraRadar.

·5 min read

Can IL-23 Drugs for Crohn's Start at Home?

Some Crohn's drugs already start with injections or a pill, but most IL-23 drugs still begin with clinic or hospital infusions. AbbVie wants to change that for Skyrizi, after its AFFIRM trial showed that starting with injections works.

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·9 min read

Approved Early, Proven Later? What Happens to Cancer Accelerated Approvals

The FDA can put a cancer drug on the market years early, on the promise that proof will follow. We checked all 219 oncology accelerated approvals on the FDA's own lists to see how often a drug with accelerated approval goes on to get full approval.

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·8 min read

How to Read a Cancer Trial and Tell If Patients Live Longer

A cancer drug 'works.' But did patients live longer, or did a tumor just shrink? The answer is which endpoint the trial made its primary measure. Here is how to read it.

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·6 min read

The Daraxonrasib Success Story

How RAS went from "undruggable" to Rasonque, the first RAS-targeted medicine to extend survival in pancreatic cancer, and the best reporting and science behind it.

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·8 min read

Can an IBD Biologic Last Six Months?

Several companies want to stretch IBD antibodies from a shot every few weeks to one every three months, or even six. Keeping the drug in the blood that long is the easy part. Whether the disease stays controlled right up to the next dose is the hard part, and the bet the newest programs are making.

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·10 min read

Does Blocking IL-17F Actually Matter?

Two of the newest PsA drugs block IL-17F as well as IL-17A; the older ones block only IL-17A. A plain walk through what the extra target actually buys: clear help on the skin, no proven help on the joints yet, and a fungal cost in the middle.

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Live data from public sources

Built on FDA approvals, ClinicalTrials.gov, SEC filings, and the Orange and Purple Books. Used by business development, competitive intelligence, medical affairs, and translational research teams across pharma and biotech.

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