Reuters · October 14, 2026
Vanda Says Drug VQW-765 Failed Main Goal of Late-Stage Social Anxiety Study; Program Put on Hold
- Vanda Pharmaceuticals said on Wednesday that its experimental drug VQW-765 for social anxiety disorder failed the main goal of a late-stage study, and that the company put the program on hold pending further analysis of the data.
- The study did not show that the drug reduced anxiety compared with placebo during a public-speaking stress test, and it also missed a key secondary goal in the broader study population, the company said.
- The trial enrolled 546 adults with social anxiety disorder at about 30 sites across the United States, according to the report.
- The study was designed to confirm findings from an earlier mid-stage trial; the late-stage results did not confirm those earlier findings, the company said.
- The company said the drug was safe and well tolerated, consistent with prior studies.
- Shares of Vanda were down about 17% in extended trading, according to the report.
Study results, enrollment and program status as stated by Vanda Pharmaceuticals, cited in the original report. Original headline: "Vanda says anxiety drug failed main goal of late-stage study, puts program on hold".
Removed: No characterization beyond the company's stated results and the reported share movement was carried.
