Millions of Americans are eagerly awaiting access to retatrutide, a powerful new drug from the pharmaceutical company. But one unidentified person has been able to gain premature access to the drug via the FDA’s “compassionate use” program, STAT reported Tuesday.
A senior clinician at the National Institutes of Health, Ranganath Muniyappa, requested access to the drug for the unnamed patient in April. Muniyappa cited a diagnosis of refractory obesity with obstructive sleep apnea and pulmonary hypertension, a potentially life-threatening disease characterized by high blood pressure in the lungs. The request reportedly drew the attention of top health officials, which STAT noted was indicative of the patient’s influence.
When asked if Trump was the 79-year-old man in question, White House spokesperson Kush Desai did not say no, and instead referred STAT to the Department of Health and Human Services. When asked if Trump had obstructive sleep apnea and pulmonary hypertension, Desai offered Trump’s latest medical evaluation as a counter, which he falsely claimed “covers this,” according to STAT. It does not—the memo makes no mention of either disease.
“The FDA supports expanded access programs that can provide patients with serious or life-threatening conditions access to investigational treatments when no comparable or satisfying approved therapies are available,” HHS spokesperson Emily Hilliard told STAT. “Each request is reviewed on a case-by-case basis based on the clinical circumstances and applicable statutory and regulatory requirements.”
Whoever the patient is, they had been previously treated with other obesity drugs such as tirzepatide, though sources who spoke with STAT indicated the patient experienced only moderate weight loss as a result. Muniyappa reportedly recommended against bariatric surgery because of the patient’s age and comorbidities.
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