Primary-outcome results across pivotal trials
Per-arm reported values from Phase 2/3 and Phase 3 trials with results posted to ClinicalTrials.gov.
| Trial | Indication | Primary endpoint | Arm | Value |
|---|---|---|---|---|
| NCT00031486 | Herpes Simplex | Survival With no or Mild Neuropsychological Impairment at 12 Months After Initiation of Study Medication as Measured by the Mattis Dementia Rating Scale (MDRS) One year post therapy. | Placebo | 2 Participants |
| Placebo | 34 Participants | |||
| Total | 7 Participants | |||
| Total | 62 Participants | |||
| Valacyclovir | 28 Participants | |||
| Valacyclovir | 5 Participants | |||
| NCT00306787 | Herpes Simplex | Investigator-assessed Time to Healing of All Non-aborted Genital Herpes Lesions 72 hours after initiation of study medication up to Day 20 | Famciclovir | 4.25 days |
| Valacyclovir | 4.08 days |