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Saturday, 15 August 2026 |
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Welcome back to another edition of Endpoints Weekly! We’re in the dog days of summer, but we still have some big stories to recap for you this weekend. Let’s break it down.
Despite keeping Robert F. Kennedy Jr.’s most extreme views at arm’s length for many months, President Donald Trump embraced some of his HHS secretary’s core claims this week. Trump signed an executive order calling for spacing out the MMR vaccine into three separate shots while falsely suggesting vaccines are linked to autism. It’s our most-read story of the week — you can find more on this from every angle below.
Elsewhere, we also covered the Phase 3 win for an oral LSD drug, a raise from an immunology biotech, a legal win for WuXi, and Sangamo’s bankruptcy auction. Have a great weekend! |
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Max Gelman |
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Senior Editor, Endpoints News |
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Trump’s MMR order |
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💉In an executive order signed Monday, President Donald Trump called for the measles, mumps and rubella (MMR) vaccine to be split into three separate shots. Trump unveiled the new order at an Oval Office event, during which he and HHS Secretary Robert F. Kennedy Jr. insinuated there was a link between vaccines and higher rates of autism.
The move creates a quandary for new CDC Director Erica Schwartz, who was confirmed last week after a yearlong vacancy for the permanent job. During her nomination hearing, Schwartz was questioned by Sen. Bill Cassidy (R-LA)
about whether she would stand up to others in the administration on vaccine policy. Cassidy was quick to criticize the new vaccine directive. “I’m a doctor. This executive order is wrong,” Cassidy wrote in a post on X, formerly Twitter. “Vaccines are overwhelmingly safe. Vaccines are effective. Vaccines DO NOT cause autism.”
Meanwhile, vaccine makers and clinical development veterans say it could take years to separate out the vaccine. Up to 10 years, to be exact, a Merck spokesperson said in a statement to Endpoints News. Read more here from Max
Bayer. |
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LSD drug clears Phase 3 test |
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💊An oral LSD drug from Definium Therapeutics succeeded in a Phase 3 trial for generalized anxiety disorder this week, the biotech announced. A single dose of the drug, called DT120, improved patients’ anxiety symptoms nearly two-fold compared to placebo on a clinician questionnaire. The result was highly statistically significant and met expectations by showing at least a five-point improvement on the symptom questionnaire.
Definium is waiting for another Phase 3 anxiety trial to produce data before filing for approval in anxiety. But the drug could also compete in major depressive disorder after it passed a Phase 3 test there in June. Should DT120 succeed in another Phase 3 depression trial, the drug would likely challenge Johnson & Johnson’s ketamine-based nasal spray Spravato. Data for the other anxiety trial are expected in September, while the second depression study should have a topline readout next year. Definium also hopes to launch a pivotal trial for post-traumatic stress disorder in 2027. |
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Boulevard Bio raises $65M |
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💰The company was unveiled on Wednesday morning with backing from Deerfield Management to advance its three immunology and inflammation (I&I) drug candidates, Kyle LaHucik wrote. Its scientific co-founders include former Sanofi R&D exec Frank Nestle and immunology professor Georg Schett.
Boulevard is already in Phase 1 in the US with an internally discovered bispecific antibody that it hopes will offer less frequent dosing and better efficacy than Vera Therapeutics’ Trutakna in IgA nephropathy. Behind BLVD101, Boulevard has a trispecific T cell engager that it hopes to send into the clinic within the next year. The company licensed the candidate from METiS TechBio, a Chinese AI drug delivery startup. |
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WuXi AppTec gets a win in court |
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🧑⚖️A federal judge has suspended the Pentagon’s designation of WuXi AppTec as a company with alleged ties to the Chinese military. Judge James Boasberg said the government’s current evidence falls short of supporting WuXi’s inclusion on the 1260H list under the US National Defense Authorization Act. WuXi sued over that designation in June, calling for “immediate removal” from the list. Boasberg’s preliminary injunction is not a final decision on WuXi’s eligibility for the list, but it temporarily blocks the government from enforcing the designation while the court case continues. |
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Sangamo’s bankruptcy auction |
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🧬The bankrupt gene editing biotech Sangamo is set to sell chunks of its business to PTC Therapeutics and Eli Lilly. The pieces will go for up to $264 million following an auction. PTC will take a Fabry disease candidate after a winning bid of $111 million upfront in cash plus up to $100 million in potential milestone payments. Lilly, meanwhile, will pay $50 million for Sangamo’s capsid delivery, zinc finger and modular integrase (MINT) platforms. It will also scoop up
the biotech’s preclinical prion disease program, known as ST-506. Read more here. |
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Worldwide made. Thanks for reading.
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