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Morning Briefing

Summaries of health policy coverage from major news organizations

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Thursday, Apr 13 2023

Full Issue

Adderall Shortage Is Causing Major Life Disruptions For Patients

Substituting a different drug doesn't always work, doctors say. And because stimulants are controlled substances, patients face extra hurdles in trying to get them: Prescriptions can’t be transferred or filled early, the Wall Street Journal reported. One patient says she called 73 pharmacies the day she ran out, to no avail.

The Wall Street Journal: As An Adderall Shortage Continues, Some Patients Put Lives On Hold

Patients say not being able to find the drugs can mean the difference between being able to work, sleep or perform daily tasks such as shopping for groceries, or not. Dr. Kathryn Boling, a family medicine doctor with Mercy Personal Physicians in Lutherville, Md., says she has combined smaller doses or swapped drugs for another stimulant. Doctors have been prescribing other stimulants such as Ritalin, Concerta and Vyvanse, to help tide over patients. “We try to help them get it in whatever way we can,” she says. (Janin, 4/13)

Vox: The Ongoing, Unnecessary Adderall Shortage, Explained

Drug shortages are almost always the result of too little supply, not too much demand. But while artificial limits on supply are undoubtedly contributing to the shortage, the growing demand for Adderall is unique. (Scott, 4/10)

In other pharmaceutical industry news —

Stat: Sickle Cell Gene Therapies Could Be Cost-Effective At $1.9 Million

As the U.S. health care system prepares for expensive gene therapies, a preliminary analysis suggests that a pair of forthcoming treatments for sickle cell disease would be cost-effective if priced as high as $1.9 million, depending upon certain variables. (Silverman, 4/12)

Stat: With FDA Staff Opposed To Sarepta Therapy, Top Official Intervened

Reviewers at the Food and Drug Administration were leaning toward rejecting a closely watched gene therapy for Duchenne muscular dystrophy made by Sarepta Therapeutics, prompting a top official to intervene earlier this year, according to three people with direct knowledge of the agency deliberations. (Feuerstein and Mast, 4/13)

Stat: Study Highlights Power Of Genetic Sequencing To Diagnose Diseases

Using genome sequencing greatly expanded the number of diagnoses researchers could provide for children with developmental disorders from thousands of families across the United Kingdom and Ireland, researchers reported in a new study Wednesday. (Joseph, 4/12)

KFF Health News: The Drug Company That Prospered Without Creating Any Drugs 

The new drug looked so promising — except for that one warning sign. At the American College of Rheumatology’s annual meeting in 2008, Duke University’s Dr. John Sundy proudly announced that pegloticase, a drug he’d helped develop, was astoundingly effective at treating severe gout, which affects perhaps 50,000 Americans. In about half of those who had taken it, the drug melted away the crystalline uric acid deposits that encrusted their joints to cause years of pain, immobility, or disfigurement. But Sundy also disclosed an unsettling detail: In one clinical trial, patients who got the drug were more likely to develop heart problems than those who didn’t. The day after Sundy’s talk, the stock price of Savient Pharmaceuticals, which developed the drug with Duke scientists, plunged 75%. (Allen, 4/13)

Stat: Pear Therapeutics Set Huge Revenue Goals — But Never Came Close

In January, Pear Therapeutics was quickly running out of money. The digital health startup embarked on an effort to sell up to $150 million worth of its stock, which could have tossed Pear a crucial lifeline as it sought to claw its way to a sustainable business. By the end of March, the stock sale had yielded just $1 million and it was evident that investors were no longer interested in funding the company. (Aguilar, 4/13)

This is part of the Morning Briefing, a summary of health policy coverage from major news organizations. Sign up for an email subscription.
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