The U.S. Food and Drug Administration has scheduled an expert advisory committee meeting for July 23-24, 2026 to consider whether licensed compounding pharmacies should be allowed to manufacture seven peptides that were placed on a restrictive list in 2023. The substances under review include BPC-157, KPV, TB-500, MOTS-c, emideltide, semax and epitalon; a second session to evaluate five more peptides is planned before the end of February 2027. Regulators cited concerns in 2023 about immunogenicity, toxicity, impurity control and scant human safety data when the group was barred from compounding. The move follows public advocacy from Health and Human Services Secretary Robert F. Kennedy Jr., who has promoted broader access to peptides and said he has used them personally. Industry groups and some compounding pharmacies have welcomed the prospect of clearer regulatory pathways, while physicians, researchers and former FDA officials warn that expanding access without robust clinical trials could expose patients to unknown risks and encourage gray‑market suppliers. The agency has highlighted manufacturing and supply chain challenges, and the Pharmacy Compounding Advisory Committee currently has multiple vacancies that could affect deliberations.

A 22-year-old woman from Manchester has been told she has about 18 months to live after a lung cancer diagnosis she and doctors link to years of vaping. Kayley Boda began using reusable vapes at 15 and switched to disposable devices shortly before symptoms began. In January 2025 she started coughing up dark brown, grainy mucus and was turned away by clinicians eight times who diagnosed chest infections. After coughing blood in March 2025 she had a chest X-ray and, following seven biopsies, was told in August 2025 she had stage one lung cancer. Surgery in September 2025 to remove the lower lobe of her right lung upstaged the disease to stage three when six lymph nodes tested positive. She underwent chemotherapy and was given the all clear in February 2026, but a pleural effusion two months later revealed the cancer had returned in the lung lining. Boda is fundraising for a clinical trial in Germany and has urged others to stop vaping. Doctors say they cannot definitively prove the cause but that smoking and vaping would not have helped her condition.

President Donald Trump on April 16–17 nominated Dr. Erica Schwartz to lead the U.S. Centers for Disease Control and Prevention, naming three senior deputies alongside her: Sean Slovenski as deputy director and COO, Dr. Jennifer Shuford as deputy director and chief medical officer, and Dr. Sara Brenner as senior counselor for public health. Schwartz, a retired rear admiral in the U.S. Public Health Service Commissioned Corps and former deputy surgeon general in Trump’s first term, is a board‑certified preventive medicine physician with medical and public‑health credentials from Brown University and the Uniformed Services University and a law degree from the University of Maryland. The nomination must be approved by the Senate; NIH director Jay Bhattacharya is serving as acting CDC director during the likely months‑long confirmation process. The pick comes after a year of turmoil at the agency — including abrupt leadership changes, staffing and budget cuts, a shooting at CDC headquarters and controversy over vaccine policy under Health Secretary Robert F. Kennedy Jr. Many public‑health experts and CDC staff greeted the selection with guarded optimism, seeing Schwartz as a conventional, experienced choice but warning her authority could be constrained by political interference.

A University College London study using UK primary care data found patients starting gabapentinoids — gabapentin or pregabalin — faced a higher risk of hospitalised drug poisoning, particularly in the first month of treatment and when the drugs were combined with benzodiazepines or opioids. Researchers analysed prescriptions in the Clinical Practice Research Datalink Aurum from 2010–2020, focusing on 16,827 people who experienced at least one drug poisoning hospitalization drawn from about 1.35 million people prescribed gabapentinoids. Compared with non-treatment periods, risk rose in the first four weeks (adjusted incidence rate ratio, aIRR 1.81). Co-prescription risk was notably higher: benzodiazepines with gabapentinoids had an aIRR of 3.95 (fourfold increase) and opioids with gabapentinoids an aIRR of 2.14 (doubling) for the first four weeks. The study also found drug-poisoning risk was elevated in the 90 days before gabapentinoid initiation (aIRR 2.09). The authors, noting the self-controlled case-series design cannot eliminate all time-varying confounding, urged clinicians to monitor patients closely at treatment initiation and avoid or minimise concurrent opioid or benzodiazepine prescribing.

A team of about 50 researchers led by Paul Verweij at Radboud University Medical Center has warned of a "silent surge" in drug-resistant fungi in a Nature Medicine paper published April 2026. The researchers — from 16 organisations worldwide — say resistance is rising in pathogens including Candida auris, azole-resistant Aspergillus fumigatus and Trichophyton indotineae. They argue that resistance often originates in the environment, driven in part by widespread agricultural use of fungicides chemically related to medical azoles, and can spread long distances via airborne spores. People with weakened immunity, such as ICU patients, transplant recipients and cancer patients, face the greatest risk; Candida auris bloodstream infections can carry high mortality. The authors set out a five-step plan calling for increased awareness, strengthened surveillance, improved infection prevention and control, optimized antifungal use, and investments in diagnostics and new drugs. They urge the inclusion of antifungal resistance in the 2026 Global Action Plan on AMR and stress the need for coordinated One Health policies linking agriculture, environment and clinical practice.

A preprint analysis and Reuters report this week found that Eli Lilly’s tirzepatide, while producing larger average weight loss than Novo Nordisk’s semaglutide, was linked with greater losses of lean body mass. The Massachusetts data‑analytics firm nference analysed roughly 1,800 tirzepatide users and about 6,200 semaglutide users, finding tirzepatide associated with an average 1.1% greater lean mass loss at three months and about 2.0% more after 12 months. The preprint categorised a “depletive GLP‑1 metabotype” (>20% total weight loss and >5% lean mass loss) in 10.3% of tirzepatide patients versus 6.7% on semaglutide in the first year. Higher doses, longer treatment and baseline musculoskeletal pain correlated with greater lean mass decline for both drugs. Separately, U.S. prescription data for the week ending April 10 show Eli Lilly’s newly approved oral weight‑loss pill Foundayo had about 1,390 prescriptions versus more than 113,000 for Novo’s Wegovy pill in the same period. Market commentary and investor notes circulated April 16–17 highlighted potential competitive and access implications as the two companies press in the global GLP‑1 market.