Research
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Insurance Stopped Covering Wegovy? What Now
Massachusetts counted about 112,000 fewer commercially insured people using weight-loss GLP-1s in early 2026 after major insurers dropped coverage. Here is why plans are cutting, what that does not mean, and what is still open.
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KPV FDA Review: What the July Vote Really Changed
KPV has never been approved as a U.S. drug. A July 2026 advisory vote favored possible 503A listing, but it did not change the list or approve a product.
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WADA Prohibited List 2027: GLP-1s Off, BPC-157 On
WADA published its 2027 list on September 21. The weight-loss drugs stay on a watch list rather than the prohibited list, the peptides stay where they were, and a prescription is still not an exemption.
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BPC-157 News Update: September 2026
A July FDA advisory vote moved the conversation forward, but it did not change the law or establish that BPC-157 works in people. A new rat study adds evidence, with the same important limit: it was not a human trial.
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Hims Peptides: What Hims & Hers Plans to Sell
Hims & Hers says a peptide and wellness category is coming, but the rollout is phased. Some offerings are planned for 2026, while BPC-157 depends on unfinished FDA rulemaking.
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What Is an IND? A Plain-English FDA Guide
An IND is the filing that lets a sponsor begin testing an investigational drug in people. It opens a research path, not a sales or prescription path.
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FDA Category 2 Bulk Drug Substances: What It Means
Category 2 means FDA has identified significant safety concerns about a nominated compounding ingredient. Here is what the category tells a patient, and why leaving it does not mean approval.
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Gray Market Peptides: What Johns Hopkins Found
Johns Hopkins says the market for unverified peptide vials is growing much faster than the human evidence. The useful question is what a prescription and a pharmacy change.
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When Was Rybelsus Approved? September 20, 2019
Rybelsus was approved on September 20, 2019. The FDA letter marked the moment a GLP-1 medicine moved from injection-only treatment into a daily tablet.
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Forzinity Approval: One Year Later
On September 19, 2025, Forzinity became the first treatment for Barth syndrome through accelerated approval. A year later, that narrow decision still rests on a required confirmatory trial.
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Is GHK-Cu FDA Approved? No, Its Review Is Pending
GHK-Cu is not FDA-approved. Its compounding review separates non-injectable use from injections, and the next advisory meeting still has no specific date.
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503B Outsourcing Facility: What the Term Means
A 503B facility can prepare compounded medicines for clinic stock under federal manufacturing rules. Its registration describes the facility, not a review of each medicine.
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FDA Tentative Approval: What It Means
FDA tentative approval means an application has cleared the scientific review needed for approval, but a legal barrier still prevents U.S. marketing. It is a real milestone, not permission to sell the drug.
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Semax FDA History: What the July Vote Changed
Semax has never had an FDA-approved U.S. product. A July 2026 advisory vote supported possible 503A listing, but it did not add Semax to the list or approve a drug.
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Tirzepatide News Update: September 2026
The month's biggest change is narrow but important: Mounjaro gained a cardiovascular-risk indication for certain adults with type 2 diabetes. Here is what else changed—and what did not.
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503B Bulks List GLP-1: Still a Proposal
FDA proposes leaving three GLP-1 ingredients off the 503B bulks list. Comments closed July 30; patient-specific prescriptions follow separate rules.
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Novo Nordisk Lilly Lawsuit: What It Doesn't Decide
The fight is about how Zepbound ads frame a head-to-head trial after a higher Wegovy dose reached the market. It is not a court verdict on which medication is better for you.
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Semaglutide News Update: September 2026
New child-trial results, heart-failure guidance, access changes and a June label update—what each means for a semaglutide prescription.
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FDA Telehealth Compounded Drugs: 5 Red Flags
FDA says telehealth sites must not present a compounded drug as a generic, a brand equivalent, or an agency-reviewed product. Here is what an honest prescription page should make clear.
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How to Get Sermorelin Prescribed: Four Steps
Getting a sermorelin prescription starts with a compound-specific medical intake, followed by a real clinician's review. Symptoms and labs can inform the decision, but neither guarantees a prescription.
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