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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 our product.

·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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·14 min read

Fifteen Drugs by Blocking. None by Switching On.

The TNF receptor superfamily has produced fifteen approved medicines, and every one of them works by shutting something down. Six receptors have been pushed the other way for twenty years, and not one agonist antibody has been approved.

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·11 min read

The Disease That Wasn't Rare After All

The scan that finds it is quick, safe, and has been around for years. Almost no cardiologist used it until a drug gave them a reason to look.

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·9 min read

IBD and Precision Medicine: Not Yet

Prometheus gave IBD its best shot at oncology-style patient selection: a companion diagnostic for its anti-TL1A drug, tulisokibart. Merck paid $10.8 billion, then built its Phase 3 trials to enroll everyone. The more crowded the anti-TL1A field gets, the stronger the case for a precision-medicine approach, even as the science has yet to deliver one.

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·6 min read

When an IBD Trial Is Terminated, the Drug Usually Didn’t Fail

Of 214 industry IBD trials terminated or withdrawn over two decades, only ~23% stopped for efficacy or safety. The rest ran out of patients, money, or corporate priority — the trial failed, not the biology.

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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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