biosimilars
Humira biosimilars are stunningly underused
Nine biosimilars for the blockbuster Humira have become available in the last year. But so far, these lower-cost alternatives to treat autoimmune diseases like rheumatoid arthritis and Crohn's disease haven't gained much traction. That's because policymakers haven't done enough to advance their uptake, opines Juliana M. Reed, executive director of the Biosimilars Forum.
Humira, these days, can cost more than $84,000 a year — and its price has increased 470% since its 2003 launch. But of the 42,000 potential Medicare beneficiaries, fewer than 1,000 received a biosimilar for the drug, she writes. Humira biosimilar competition accounts for less than 2% of the market, even though their prices can be as much as 85% lower.
But PBMs continue to favor the branded version of the biologic, making it easier for patients to access. Some PBMs even deny biosimilars outright without any explanation. To change this, policymakers need to step up: They need to crack down on anti-competitive schemes from PBMs, Reed writes, and prioritize patient access to affordable drugs.
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rabies
Replicate's srRNA rabies vaccine effective in Phase 1
San Diego-based Replicate Bioscience, a clinical stage company, reported Wednesday that its self-replicating RNA (srRNA) rabies vaccine induced strong immune responses in a Phase 1 clinical trial, even at extremely low doses — doses that contained fractions of the volume found in messenger RNA Covid vaccines on the market.
The company reported that at all three doses tested — which went from 10 micrograms, a third of the volume of Pfizer's Covid vaccine, down to an ultra-low 0.1 micrograms — the experimental vaccine induced neutralizing antibody titers at levels that exceeded the World Health Organization's defined surrogate level of protection for rabies virus. (Replicate's press release said "most" recipients of the 0.1 mcg-dose arm generated antibody titer levels that met the WHO's standard.) The vaccine, RB1-4000, was well tolerated at all doses tested, with no severe adverse events among the 84 people in the trial. "These results have exceeded our expectations and show the power and potential of our srRNA technology," CEO Nathaniel Wang said.
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