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  1. pharmadog
  2. ›drugs
  3. ›IVERMECTIN
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IVERMECTIN

Marketedupdated 5mo ago
by Mountain Valley MD Holdings Inc
Approved
community read0 votes

🐶 often sniffed alongside

top 5
  • tagApproval6 co-mentions · 3 sources
  • drugMDC-STM3 co-mentions · 3 sources
  • tagSmall Molecule3 co-mentions · 3 sources
  • companyZydus Lifesciences Ltd1 co-mentions · 1 sources
  • companyAjanta Pharma Ltd1 co-mentions · 1 sources

all catalysts(2)

approval · 2
Feb 26, 2026
approval
7mo ago
IVERMECTIN — FDA approval
IVERMECTIN
→
Apr 7, 2026
approval
6mo ago
IVERMECTIN — FDA approval
IVERMECTIN
→

Trials studying IVERMECTIN

  • phase1A Study Comparing Ivermectin Cream 1%, Soolantra™ Cream 1%, PrROSIVER® Cream1% to Placebo Control in the Treatment of Moderate to Severe Facial Rosacea.completedn=865
  • phase2Ivermectin in Combination With Balstilimab or Pembrolizumab in Patients With Metastatic Triple Negative Breast Cancerrecruitingn=34
  • phase3COVID-OUT: Early Outpatient Treatment for SARS-CoV-2 Infection (COVID-19)completedn=1,323
  • phase2Rosacea and Ivermectincompletedn=30
  • phase3Evaluation of Effectiveness of ALBENDAZOLIVERMECTIN Coformulation vs ALBENDAZOLE for Treatment of Intestinal Wormsterminatedn=1,001
  • phase2A Study to Evaluate the Efficacy and Safety of Ivermectin in COVID-19 Preventioncompletedn=400
  • phase1Bioequivalence Study of Ivermectin 1% Cream and Soolantra (Ivermectin) 10 mg/g Creamcompletedn=44
  • phase2Emodepside Phase II Trial for Treatment of Onchocerciasisactive not recruitingn=578

Patent cliff

source: FDA Orange Book
first barrier falls
Mar 13, 2034
~7.4 years out

Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.

patents (5)

  • Mar 13, 2034method-of-use (U-1631)US 10206939
  • Mar 13, 2034method-of-use (U-1631)US 9089587
  • Mar 13, 2034method-of-use (U-1631)US 9233117
  • Mar 13, 2034method-of-use (U-1631)US 9233118
  • Mar 13, 2034method-of-use (U-1631)US 9782425

News(6)

  • FDA Issues Emergency Use Authorization for Generic Drug to Prevent New World Screwworm in Cattle
    FDA issues Emergency Use Authorization (EUA) for Bimectin (ivermectin) injection for the prevention of New World screwworm (NWS) infestations (myiasis) in cattle when administered within 24 hours o…
    fda_press · 1mo ago
  • FDA Issues Emergency Use Authorization for Drug for Short-Term Prevention of New World Screwworm in Horses
    The FDA today issued an Emergency Use Authorization (EUA) for Ivermectin Liquid for Horses (ivermectin oral solution) for the short-term prevention of New World screwworm (NWS) infestations (myiasi…
    fda_press · 2mo ago
  • Tennessee pharmacies sell potent ivermectin, led by anti-vaccine doctor who’s taken ‘bucketloads’
    Tennessee pharmacies are selling potent versions of the antiparasitic drug ivermectin, led by an anti-vaccine doctor who’s taken "bucketloads."
    stat · 3mo ago
  • The connection between periods and mental health
    Plans to oust Makary, a looming Supreme Court deadline on mifepristone, and other health news from Morning Rounds
    stat · 4mo ago
  • Opinion: I’m fighting misinformation online. False hantavirus claims follow a now-familiar playbook
    The cruise ship hantavirus outbreak is serious but limited. Online, it's another story.
    stat · 4mo ago
  • Opinion: The podcast telling the stories behind Ambien, Ozempic, EpiPens, and other game-changing drugs
    “We're basically not using our body as directed,” says "Drug Story" host Thomas Goetz.
    stat · 5mo ago
brand
IVERMECTIN
generic
IVERMECTIN
indication
Coronavirus Disease 2019 (COVID-19)
phase
marketed
Data sources
openFDA · ClinicalTrials.gov
last refreshed 4h ago
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