Recent Updates
Recently added Catalysts

Duragesic/h+ Scotch Duct Tape

Phase 1

Healthy | Small molecule | Other |Viatris Inc.|Last Updated: Apr 23, 2024

Success Probability

Subscribe to view

Market & Valuation

Subscribe to view

Trial Design

RandomizedCONTROLLEDBiomarker
Total Trials1
Total Enrollment12

FDA Designations

No designations recorded

Clinical trial landscape

Duragesic/h+ Scotch Duct Tape · 1 trial · 1 indication

Phase 1 1
NCT00650117Bioequivalence and Wear Study of Mylan Fentanyl Transdermal System 25 µg/h and Mylan Fentanyl Transdermal SystemHealthy
COMPLETED12 Analytics
PHASE1COMPLETED
Bioequivalence and Wear Study of Mylan Fentanyl Transdermal System 25 µg/h and Mylan Fentanyl Transdermal System
HealthyUnlock trial analytics

Study Endpoints

Primary Endpoints

Drug Delivery
within 30 days
Unlock Study Endpoints

Study Design & Arms

AllocationRANDOMIZED
MaskingNONE
ModelPARALLEL
PurposeOTHER

Treatment Arms

ArmTypeDescription
1EXPERIMENTALMylan Fentanyl Transdermal System 25 mcg/h + Scotch Duct Tape (3M)
2EXPERIMENTALMylan Fentanyl Transdermal System 25 mcg/h + Blenderm Clear Plastic Surgical Tape (3M)
3EXPERIMENTALMylan Fentanyl Transdermal System 25 mcg/h + Microfoam Tape (3M)
4EXPERIMENTALDuragesic 25 mcg/h + Scotch Duct Tape (3M)
5EXPERIMENTALDuragesic 25 mcg/h + Blenderm Clear Plastic Surgical Tape (3M)
6EXPERIMENTALDuragesic 25 mcg/h + Microfoam Tape (3M)

Interventions

NameTypeDescription
Mylan Fentanyl Transdermal System 25 mcg/h + Scotch Duct Tape (3M)DRUGsingle application
Duragesic 25 mcg/h + Scotch Duct Tape (3M)DRUGsingle application
Mylan Fentanyl Transdermal System 25 mcg/h + Blenderm Clear Plastic Surgical Tape (3M)DRUGsingle application
Duragesic 25 mcg/h + Blenderm Clear Plastic Surgical Tape (3M)DRUGsingle application
Mylan Fentanyl Transdermal System 25 mcg/h + Microfoam Tape (3M)DRUGsingle application
Duragesic 25 mcg/h + Microfoam Tape (3M)DRUGsingle application
Unlock Study Design Details

Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersYes
Study Sites1

Inclusion Criteria: 1. Age: 18 years and older. 2. Sex: Male and/or non-pregnant, non-lactating female. 1. Women of childbearing potential must have negative serum beta human chorionic gonadotropin (beta-HCG) pregnancy tests performed within 21 days prior to the start of the study and on the ev...

Countries:United States
Unlock Eligibility Criteria

Frequently asked questions about Duragesic/h+ Scotch Duct Tape

What is Duragesic/h+ Scotch Duct Tape?

Duragesic/h+ Scotch Duct Tape is a small molecule drug being developed by Viatris Inc. (VTRS). It is currently in Phase 1 clinical development for use in healthy volunteers. The drug is being studied in a bioequivalence and wear study of the Mylan Fentanyl Transdermal System.

What is Duragesic/h+ Scotch Duct Tape used for?

Duragesic/h+ Scotch Duct Tape is being studied for use in healthy volunteers. The ongoing clinical trial is a bioequivalence and wear study of the Mylan Fentanyl Transdermal System 25 µg/h. It is an investigational drug still in clinical development and has not been approved for any indication.

Who makes Duragesic/h+ Scotch Duct Tape?

Duragesic/h+ Scotch Duct Tape is being developed by Viatris Inc., which trades under the ticker VTRS. The company is conducting a Phase 1 clinical trial to evaluate the drug in healthy volunteers.

What phase is Duragesic/h+ Scotch Duct Tape in?

Duragesic/h+ Scotch Duct Tape is in Phase 1 clinical development. The drug is investigational and has not been approved by regulatory authorities. One Phase 1 trial has been completed, and there are no active trials currently.

What clinical trials is Duragesic/h+ Scotch Duct Tape in?

Duragesic/h+ Scotch Duct Tape has one completed clinical trial, NCT00650117, titled "Bioequivalence and Wear Study of Mylan Fentanyl Transdermal System 25 µg/h and Mylan Fentanyl Transdermal System." This Phase 1 study enrolled 12 healthy volunteers in the United States and was controlled and randomized.