Latigo's mid-stage trial shows non-opioid pill LTG-001 cuts post-surgery pain, outperforms placebo
Latigo Biotherapeutics reported positive Phase 2 data for its experimental oral analgesic LTG-001, tested in patients who had undergone tummy-tuck surgery. The study enrolled 343 participants who were randomly assigned to high or low doses of the drug, a placebo, or a standard acetaminophen-hydrocodone combination.
Both dose levels of LTG-001 produced statistically significant pain reduction at the 48-hour mark compared with placebo. Moreover, patients receiving the higher dose were markedly less likely to request rescue oxycodone than those on placebo.
The safety profile appeared favorable, with the drug being well tolerated and no major adverse events reported. The results suggest LTG-001 could become a non-opioid alternative for acute postoperative pain, positioning Latigo to compete with Vertex’s existing pain therapy.
This writeup was produced by pharmadog from original reporting by STAT.
Original headline: “STAT+: Latigo reports mid-stage success for would-be rival to Vertex’s pain drug Journavx”
read at STAT ↗
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