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VX-548 Significantly Reduces Moderate to Severe Acute Pain, Phase III Program Data Reveal

VX-548 demonstrated a more rapid onset to meaningful pain relief post-surgery compared with placebo.

Jessica oswaldReshma kewalramaniUniversity of california san diegoVertex acute pain steering committeePain intensity differenceNumeric pain rating scalePatient global assessmentEmergency medicinePain medicineCalifornia san diego

Sorrento Therapeutics (SRNEQ) Announces Positive Phase 2a Clinical Trial Results for Resiniferatoxin

Sorrento Therapeutics (SRNEQ) Announces Positive Phase 2a Clinical Trial Results for Resiniferatoxin
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Henry jiContactalexis nahamaSemnur pharmaceuticals incBankruptcy court the chapterExchange commissionSorrento therapeutics ark animal healthBankruptcy courtSorrento therapeutics incScilex pharmaceuticals incPivotal trialc le ar programSorrento therapeuticsLine safety outcomesLine efficacyDurability outcomesPain intensity differenceChief executive

Sorrento Therapeutics Announces Positive Phase 2a Clinical Trial Results for Resiniferatoxin (RTX) for the Treatment of Knee Pain in Moderate to Severe Osteoarthritis of the Knee (OAK) Patients

Sorrento Therapeutics Announces Positive Phase 2a Clinical Trial Results for Resiniferatoxin (RTX) for the Treatment of Knee Pain in Moderate to Severe Osteoarthritis of the Knee (OAK) Patients
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Henry jiAlexis nahamaBankruptcy court the chapterSemnur pharmaceuticals incScilex pharmaceuticals incSorrento therapeutics incExchange commissionBankruptcy courtSorrento therapeutics ark animal healthPivotal trialc le ar programSorrento therapeuticsLine safety outcomesLine efficacyDurability outcomesPain intensity differenceChief executive

Oral NaV1 8 Inhibitor Designated Breakthrough Tx for Severe Acute Pain

The Food and Drug Administration has granted Breakthrough Therapy designation to VX-548 for the treatment of moderate to severe acute pain.

Carmen bozicGlobal medicines developmentVertex pharmaceuticals incDrug administrationBreakthrough therapyPain intensity differenceExecutive vice presidentMedical affairsChief medical officer

Oral NaV1 8 Inhibitor Designated Breakthrough Tx for Severe Acute Pain

The Food and Drug Administration has granted Breakthrough Therapy designation to VX-548 for the treatment of moderate to severe acute pain.

Carmen bozicGlobal medicines developmentDrug administrationBreakthrough therapyPain intensity differenceExecutive vice presidentMedical affairsChief medical officer