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Five-Year Safety Study of Pimecrolimus Cream 1% in Infants 3 to Less Than 12 Months of Age with Mild to Moderate Atopic Dermatitis - Article


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Dermatitis

Types of dermatitis; Contact Dermatitis; Dermatitis-Atopic Eczema; Dermatitis/Eczema; Rash; Skin Disorders, Dermatitis; Skin Rash; Slide Show: Types of Dermatitis




Clinical Trial: Five-Year Safety Study of Pimecrolimus Cream 1% in Infants 3 to Less Than 12 Months of Age with Mild to Moderate Atopic Dermatitis

This study is currently recruiting patients.

Sponsored by: Novartis
Information provided by: Novartis

Purpose

The primary purpose of this study is to investigate the safety of pimecrolimus cream 1% in the long-term treatment (up to 5 years) of atopic dermatitis (eczema) in patients less than 12 months of age compared to topical corticosteroids (TCS).
Condition Intervention Phase
Atopic Dermatitis
 Drug: Pimecrolimus cream 1%
Phase III

MedlinePlus related topics:  Allergy;   Dermatitis;   Genetic Disorders;   Skin Diseases

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study

Further Study Details: 

Study start: April 2004

Eligibility

Ages Eligible for Study:  3 Months   -   12 Months,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • Diagnosis of AD fulfilling the diagnostic criteria of Seymour
  • AD affecting at least 5% total body surface area
  • Investigator’s Global Assessment (IGA) score of 2 or 3, corresponding to mild-to-moderate disease at baseline

Exclusion Criteria:

  • Phototherapy, systemic therapy (e.g., immunosuppressants, cytostatics), systemic corticosteroids within 4 weeks
  • Topical tacrolimus or pimecrolimus within 2 weeks
  • Topical therapy (e.g., tar, topical corticosteroids) within 3 days
  • Immunocompromised (e.g., lymphoma, AIDS, Wiskott-Aldrich Syndrome) or have a history of malignant disease
  • Active acute viral skin infection (e.g. herpes simplex, herpes zoster, chicken pox), and/or clinically infected AD
  • Failure to thrive (e.g., weight or height/length below the 5th percentile) or developmental abnormalities such as head circumference less than 5th and more than 95th percentile
  • Known hypersensitivity to any ingredient of pimecrolimus cream 1% cream 1% or topical corticosteroids

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00120523

Customer Information Center      862-778-8300 

Arizona
      Phoenix Children’s Hospital, Phoenix,  Arizona,  85016,  United States; Recruiting
Judy O’Haver  602-546-0895 
Ronald C Hansen,  Principal Investigator

      Cholla Pediatrics, TUSCON,  Arizona,  85741,  United States; Recruiting
Eileen Davis  520-544-7650 
Kevin Concannon,  Principal Investigator

Arkansas
      Arkansas Pediatric Clinic, Little Rock,  Arkansas,  72205,  United States; Recruiting
Shelley Marti  501-661-0308  Ext. 130 
Anthony D Johnson,  Principal Investigator

      Little Rock Allergy & Asthma Clinic, Little Rock,  Arkansas,  72205,  United States; Recruiting
Mindy DeMarco  501-224-7147 
Karl V Sitz,  Principal Investigator

California
      Pediatric Care Medical Group, Inc., Huntington Beach,  California,  92647,  United States; Recruiting
Jennifer Cardona  714-842-1441 
Paul Y Qaqundah,  Principal Investigator

      9540 Artesia Blvd., Suite #1, Bellflower,  California,  90706,  United States; Recruiting
Eileen Vergara  562-925-2625 
Victoria Sanchez-Bal,  Principal Investigator

Colorado
      Longmont Clinical Research, Longmont,  Colorado,  80501,  United States; Recruiting
Stacy Cecil  303-776-8718 
Scott D Clark,  Principal Investigator

Florida
      Children’s Skin Center, Miami,  Florida,  33155,  United States; Recruiting
Mirta Caminero  305-669-6555 
Ana M Duarte,  Principal Investigator

      Pediatric Research Center of South Florida, Palm Beach Gardens,  Florida,  33458,  United States; Recruiting
Joan Wilder  561-745-4215 
Tommy J Schechtman,  Principal Investigator

Georgia
      The Pediatric Center, Stone Mountain,  Georgia,  30083,  United States; Recruiting
Kathleen Allen  404-269-3800 
Jaquelin Gotlieb,  Principal Investigator

      AeroAllergy Research Laboratories of Savanah, Inc., Savannah,  Georgia,  31406,  United States; Recruiting
Susie Kitchen  912-356-3619 
Brad Goodman,  Principal Investigator

Michigan
      Michigan State University – Kalamazoo Center for Med Studies, Kalamazoo,  Michigan,  49008,  United States; Recruiting
Karyl Hare  269-337-6450 
Douglas Homnick,  Principal Investigator

      Respiratory Medicine Research Institute of Michigan, Ypsilanti,  Michigan,  48197,  United States; Recruiting
Patricia Lezak  734-434-3007 
Jeffrey G Leflein,  Principal Investigator

      Wayne State University Dermatology, Detroit,  Michigan,  48201,  United States; Recruiting
Loretta Grimillion  313-577-5057 
Robert Schoenfeld,  Principal Investigator

Minnesota
      Dermatology Center for Children, Minneapolis,  Minnesota,  55404,  United States; Recruiting
Dawn Larson  612-863-8563 
Kenneth E Bloom,  Principal Investigator

      University of Minnesota – Dept. of Dermatology, Minneapolis,  Minnesota,  55455,  United States; Recruiting
Cathy Boeck  612-625-4973 
Maria Hordinsky,  Principal Investigator

      SMDC Health System, Duluth,  Minnesota,  55805,  United States; Recruiting
Laurie Athmann  218-786-8363 
Nancy Monaghan-Beery,  Principal Investigator

Missouri
      Radiant Research, Bridgeton,  Missouri,  63044,  United States; Recruiting
Sarah Conell  314-344-7337 
Craig Spiegel,  Principal Investigator

New York
      Dermatology Associates of Rochester, P.C., Rochester,  New York,  14623,  United States; Recruiting
Chris Englert  585-272-0700 
Robert W Loss, Jr.,  Principal Investigator

North Carolina
      Capitol Pediatrics & Adolescent Center, Raleigh,  North Carolina,  27609,  United States; Recruiting
Judy Mulvihill  919-782-5273 
Linda Butler,  Principal Investigator

Ohio
      Dermatology Research Associates, Cincinnati,  Ohio,  245230,  United States; Recruiting
Diana Crowthers  513-232-3376 
Anne W Lucky,  Principal Investigator

      Ohio Pediatrics, Inc., Huber Heights,  Ohio,  45424,  United States; Recruiting
Janet Tokers  937-236-5396 
Julie Shepard,  Principal Investigator

Oregon
      The Portland Clinic, Beaverton,  Oregon,  97006,  United States; Recruiting
Nancy Chess  503-221-0161 
Mary Ellen Ulmer,  Principal Investigator

      Calcagno Research and Development, Gresham,  Oregon,  97030,  United States; Recruiting
Carisa Reynolds  503-491-0714 
John A Calcagno,  Principal Investigator

South Carolina
      Allergy & Asthma Consultants, LLP, Charleston,  South Carolina,  29414,  United States; Recruiting
Arlene Conte  843-556-9588 
Thomas B Harper, III,  Principal Investigator

      Allergic Disease and Asthma Center, Greenville,  South Carolina,  29607,  United States; Recruiting
Linda Erwin  864-627-3800 
Neil L Kao,  Principal Investigator

Tennessee
      University of Tennessee – Dept. of Pediatrics, Memphis,  Tennessee,  38105,  United States; Recruiting
Kim Fisher  901-572-5345 
Andrew Spooner,  Principal Investigator

Texas
      Suzanne Bruce& Associates, PA, Houston,  Texas,  77056,  United States; Recruiting
Maria Crockett  713-850-0240 
Suzanne Bruce,  Principal Investigator

      Grand Parkway Pediatrics, Sugar Land,  Texas,  77479,  United States; Recruiting
Nanci Hadash  281-494-8687 
Michael Bishop,  Principal Investigator

Virginia
      Virginia Commonwealth University, Richmond,  Virginia,  23298,  United States; Recruiting
Tammy Anderson  804-827-1856 
Anne Marie Irani,  Principal Investigator

More Information

Study ID Numbers:  ASM981C2306
Record last reviewed:  July 2005
Last Updated:  July 21, 2005
Record first received:  July 15, 2005
ClinicalTrials.gov Identifier:  NCT00120523
Health Authority: United States: Food and Drug Administration; Argentina: Administracion Nacional de Medicamentos, Alimentos y Tecnologia Medica; Belgium: Directorate general for the protection of Public health: Medicines; Canada: Health Canada; Chile: Instituto de Salud Publica de Chile; China: State Food and Drug Administration; Colombia: INVIMA Instituto Nacional de Vigilancia de Medicamentos y Alimentos; Czech Republic: State Institute for Drug Control; Finland: National Agency for Medicines; Germany: Federal Institute for Drugs and Medicinal Devices; Greece: National Organization of Medicines; Hong Kong: Department of Health; Netherlands: Medicines Evaluation Board (MEB); Peru: General Directorate of Pharmaceuticals, Devices, and Drugs; Portugal: National Pharmacy and Medicines Institute; Poland: Ministry of Health; Russia: Pharmacological Committee, Ministry of Health; Singapore: Health Sciences Authority; South Africa: Medicines Control Council; Spain: Spanish Agency of Medicines; Sweden: Medical Products Agency; Taiwan: Department of Health; Turkey: Ministry of Health; United Kingdom: Medicines and Healthcare Products Regulatory Agency
ClinicalTrials.gov processed this record on 2005-07-26

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December 4, 2008



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