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Mylan Fentanyl System/h+ Scotch Duct Tape

Phase 1

Undisclosed | Small molecule | Other |Viatris Inc.|Trials Updated: Apr 23, 2024

Success Probability

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Market & Valuation

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Trial Design

RandomizedCONTROLLED
Total Trials1
Total Enrollment12

FDA Designations

No designations recorded

Mylan Fentanyl System/h+ Scotch Duct Tape clinical trials

Mylan Fentanyl System/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
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Study Endpoints

Primary Endpoints

Drug Delivery
within 30 days
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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
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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
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Frequently asked questions about Mylan Fentanyl System/h+ Scotch Duct Tape

What is Mylan Fentanyl System/h+ Scotch Duct Tape?

Mylan Fentanyl System/h+ Scotch Duct Tape refers to a Mylan fentanyl transdermal system, a small molecule patch, evaluated in a Phase 1 study alongside Scotch Duct Tape from 3M. The trial examined bioequivalence and wear of the Mylan Fentanyl Transdermal System 25 mcg/h in healthy adult volunteers.

Who makes Mylan Fentanyl System/h+ Scotch Duct Tape?

Viatris Inc., which trades under the ticker VTRS, is the developer associated with the Mylan Fentanyl Transdermal System. The product name reflects Mylan, a Viatris brand, and the Scotch Duct Tape referenced in the study is a 3M product.

What phase is Mylan Fentanyl System/h+ Scotch Duct Tape in?

Mylan Fentanyl System/h+ Scotch Duct Tape is in Phase 1 development. One Phase 1 trial has been completed, and no trials are currently active. The study enrolled 12 healthy adult volunteers in the United States.

What clinical trials is Mylan Fentanyl System/h+ Scotch Duct Tape in?

Mylan Fentanyl System/h+ Scotch Duct Tape was studied in one completed Phase 1 trial, NCT00650117, titled Bioequivalence and Wear Study of Mylan Fentanyl Transdermal System 25 mcg/h and Mylan Fentanyl Transdermal System. It was a controlled, randomized study with 12 healthy volunteers in the United States.