We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov Menu

Study of orBec® With Prednisone Therapy in the Treatment of Patients With Graft Versus Host Disease (GVHD) (SUPPORTS)

This study has been terminated.
(An independent Data Safety Monitoring Board recommended the study be stopped due to futility)
ClinicalTrials.gov Identifier:
First Posted: June 23, 2009
Last Update Posted: December 6, 2013
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Use of an oral topically-active glucocorticoid with limited side effects will control the gastrointestinal inflammatory process of GVHD and minimize glucocorticoid exposure.

Condition Intervention Phase
Acute Gastrointestinal Graft vs Host Disease Drug: oral beclomethasone 17,21-dipropionate Drug: Placebo Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of the Safety and Efficacy of orBec® (Oral Beclomethasone 17,21-Dipropionate)in Conjunction With Ten Days of High-Dose Prednisone Therapy in the Treatment of Patients With Gastrointestinal GVHD

Resource links provided by NLM:

Further study details as provided by Soligenix:

Primary Outcome Measures:
  • The Proportion of Subjects With GVHD Treatment Failure [ Time Frame: Day 80 ]
    The primary endpoint is the occurrence (yes, no) during the 80-day study period of GVHD treatment failure defined as use of prednisone or equivalent IV corticosteroids at doses higher than stated in the protocol, or use of any additional other glucocorticoid (including unblinded BDP) or addition of other immunosuppressant medications, in response to uncontrolled signs or symptoms of GVHD

Secondary Outcome Measures:
  • Cumulative Exposure to Prednisone [ Time Frame: Day 80 ]
  • Survival Status [ Time Frame: Day 200 ]

Enrollment: 140
Study Start Date: October 2009
Study Completion Date: May 2012
Primary Completion Date: December 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: orBec®
Investigational drug
Drug: oral beclomethasone 17,21-dipropionate
Two tablets QID for 50 days
Other Names:
  • orBec
  • BDP
Placebo Comparator: Placebo
Drug: Placebo
Two tablets QID for 50 days


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Receipt of allogeneic hematopoietic cell transplant
  • Diagnosis of GI graft vs. host disease (GVHD)
  • No GI infection
  • Must be able to swallow tablets
  • Must be able to read and understand informed consent
  • Adequate birth control methods for the duration of the study

Exclusion Criteria:

  • Significant Skin GVHD
  • Liver GVHD
  • Persistent vomiting
  • HIV positive
  • Pregnancy/lactation
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00926575

United States, New York
Buffalo, New York, United States
United States, North Carolina
Durham, North Carolina, United States
United States, Washington
Seattle, Washington, United States
Sponsors and Collaborators
Principal Investigator: Keith Sullivan, MD Duke University
Principal Investigator: David Hockenbery, MD Fred Hutchinson Cancer Research Center
  More Information

Responsible Party: Soligenix
ClinicalTrials.gov Identifier: NCT00926575     History of Changes
Other Study ID Numbers: BDP-GVHD-03
First Submitted: June 19, 2009
First Posted: June 23, 2009
Results First Submitted: July 12, 2013
Results First Posted: December 6, 2013
Last Update Posted: December 6, 2013
Last Verified: August 2013

Keywords provided by Soligenix:
beclomethasone dipropionate
bone marrow transplant
hematopoietic cell transplant
stem cell transplant
marrow transplant
beclomethasone 17,21-dipropionate

Additional relevant MeSH terms:
Graft vs Host Disease
Immune System Diseases
Anti-Inflammatory Agents
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Antineoplastic Agents, Hormonal
Antineoplastic Agents
Anti-Asthmatic Agents
Respiratory System Agents