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Trial · Interventional

CompletedPhase 2Registry data

Safety and Efficacy of ALX-0600 in Subjects With Active Crohn's Disease

Overview

Status
Completed
Phase
Phase 2
Enrollment
100 participants (actual)
Sponsor
Shire · Industry
Design
Randomized · Triple masking
Countries
2 countries

United States, Canada

Start
12 Nov 2003
Primary completion
28 Jul 2005
Completion
28 Jul 2005
First posted
13 Nov 2003 (estimated)
Last update posted
25 May 2021
Conditions
Crohn's Disease

Timeline

1 trial · 1 completed

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
2003200420052006
  1. Ph 2

    Safety and Efficacy of ALX-0600 in Subjects With Active Crohn's Disease

    NCT00072839

    12 Nov 2003 to 28 Jul 2005

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

The purpose of the study is to determine whether an investigational compound, ALX-0600, is safe and effective in treating Crohn's Disease.

Interventions

  • ALX-0600Drug
  • placeboDrug
  • teduglutide 0.05Drug
  • teduglutide 0.2 mgDrug
  • Teduglutide 0.05 doseDrug
  • teduglutide 0.1 mg doseDrug

Arms4

  • Placebo comparator

    Placebo

    placebo solution injected subcutaneously daily into either thigh or abdomen.

  • Experimental

    teduglutide 0.05

    teduglutide 0.05 mg/kg/d injected subcutaneously daily.

  • Experimental

    teduglutide 0.1

    0.1 mg/kg/d teduglutide injected subcutaneously into thigh or abdomen

  • Experimental

    teduglutide

    0.2 mg/kg/d teduglutide injected subcutaneously into thigh or abdomen

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. The primary efficacy variable is the percentage of subjects who respond to treatment, defined as the percentage of subjects who are in remission (CDAI less than 150) or have a 100-point or greater reduction from baseline in CDAI score at dosing Week 8.

    Time frame · 8 weeks of treatment

Secondary outcomes(1)
  1. The various secondary efficacy variables are based on the CDAI, Inflammatory Bowel Disease Questionnaire (IBDQ), plasma citrulline and laboratory inflammatory markers.

    Time frame · 8 weeks of treatment

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

No results are posted for this trial.

Completed trials do not always post results.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies1

Studies that cite this trial.

Studies with results

1 study on this page

Indexing hint: Randomized controlled trial · 2010

7 results

Teduglutide, a novel mucosally active analog of glucagon-like peptide-2 (GLP-2) for the treatment of moderate to severe Crohn's disease.

Buchman et al. 2010Inflammatory bowel diseasescited by 109

PMID 19821509DOI 10.1002/ibd.21117PUB-19821509

Full text at the publisher7 results

Eligibility

Who could join, as posted.

Sex
All
Age
from 18 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria 1. Men and women, 18 years of age and older 2. Signed and dated informed consent to participate before any study-related procedures are performed 3. Diagnosis of Crohn's disease for at least 6 months that has been documented and confirmed 4. A Crohn's Disease Activity Index (CDAI) score of 220 to 450 inclusive 5. Female subjects who are not surgically sterile or postmenopausal must use medically acceptable methods of birth control during and for 30 days after the treatment period. 6. HCT 30% or greater 7. WBC 3.5 x 109/L or greater 8. Platelets 100 x 109/L or greater 9. Adequate renal function defined as: serum creatinine and BUN 1.5 x ULN or less 10. Adequate hepatic function defined as: ALT/SPGT, AST/SGOT 2.0 x ULN or less; total bilirubin 1.25 x ULN or less, alkaline phosphatase 1.5 x ULN or less 11. Female subjects of childbearing potential must have negative urine pregnancy test results prior to randomization 12. A stool sample must be taken at screening and analyzed by a local laboratory for enteric pathogens, pathogenic ova and parasites, and Clostridium difficile toxin, and reported negative prior to randomization. 13. C-reactive protein value must be 1.0 mg/dL or more, unless there are obvious manifestations of currently active Crohn's disease such as positive observations on endoscopy, other positive indications by laboratory test results, or the subject has had a previous intestinal resection for Crohn's disease. Exclusion Criteria 1. Nutritionally compromised subjects requiring enteral or parenteral therapy to maintain weight 2. Body weight less than 40 kg or more than 100 kg 3. Bowel obstruction or any condition that may predispose to its development, intestinal perforation, or significant gastrointestinal hemorrhage 4. Current ileostomy or colostomy or extensive external fistulization (more than 3 external fistulae which are expressible with gentle compression) 5. Expected to require surgical therapy for Crohn's disease or Crohn's disease related complications within 12 weeks of screening. If an abscess is present, it should be drained at least 3 weeks before pre-screening 6. History of ulcerative colitis within 6 months of screening visit 7. Cushing's syndrome 8. Known HIV infection, or symptoms or signs of HIV infection 9. Acute systemic infection and/or intestinal infection requiring antibiotic therapy at time of screening or baseline 10. Evidence of chronic hepatitis B or C viral infection 11. Decompensated liver disease 12. Clinically significant ECG abnormalities 13. History of angina or cardiac arrhythmia requiring drug or device intervention or clinically significant congestive heart failure or other clinically significant cardiac disease 14. History of myocardial infarction within 12 months of screening 15. History of thromboembolic disease (e.g., phlebitis, pulmonary embolus) or known congenitally or acquired prothrombotic disorder (e.g., protein C deficiency) 16. History of cancer (other than resected cutaneous basal or squamous cell carcinoma or in situ cervical cancer) or clinically significant lymphoproliferative disease with fewer than 5 years documented disease-free state 17. Known substance abuse in the previous 2 years 18. Nursing mothers or pregnant women 19. Use of native GLP-2, growth hormone, or growth factors within 3 months of signing informed consent 20. Use of any of the prior or concomitant medications described in section 5.4, except as specified 21. Known hypersensitivity to any of the active or inactive constituents of ALX-0600

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