Activity & Safety Study of KX2-391 Ointment in Participants With Actinic Keratosis on the Face or Scalp

PHASE2CompletedINTERVENTIONAL
Enrollment

168

Participants

Timeline

Start Date

April 11, 2016

Primary Completion Date

January 11, 2017

Study Completion Date

December 22, 2017

Conditions
Actinic Keratosis
Interventions
DRUG

50 mg of KX2-391 Ointment 1%

Dose: 50 mg; Route of administration: Topical

DRUG

50 mg of KX2-391 Ointment 1%

Dose: 50 mg; Route of administration: Topical

Trial Locations (16)

29414

Dermatology and Laser Center of Charleston, Charleston

32806

Compass Research, Orlando

33134

Clinical Research of South Florida, Coral Gables

33144

International Dermatology Research, Miami

33409

Palm Beach Research Center, West Palm Beach

33624

Forward Clinical Trials, Inc., Tampa

37130

Institute of Clinical Research - Tennessee, LLC, Murfreesboro

55432

Minnesota Clinical Study Center, Fridley

77056

The Center for Skin Research, Houston

77845

J&S Studies, Inc., College Station

78229

Clinical Trials of Texas, Inc., San Antonio

Dermatology Clinical Research Center, San Antonio

80220

Horizons Clinical Research Center, Denver

91942

eStudy Site, La Mesa

92262

Palmtree Clinical Research, Inc., Palm Springs

94538

Center for Dermatology Clinical Research, Fremont

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Athenex, Inc.

INDUSTRY

lead

Almirall, S.A.

INDUSTRY

NCT02838628 - Activity & Safety Study of KX2-391 Ointment in Participants With Actinic Keratosis on the Face or Scalp | Biotech Hunter | Biotech Hunter