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Safety, Tolerability and Efficacy of ATL-104 in Oral Mucositis

Primary Purpose

Mucositis

Status
Completed
Phase
Phase 2
Locations
United Kingdom
Study Type
Interventional
Intervention
ATL-104
Sponsored by
Alizyme
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Mucositis focused on measuring Mucositis, Peripheral blood stem cell transplant

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients with haematological malignancies undergoing chemotherapy in association with PBSCT Exclusion Criteria: Clinically significant conditions that would exclude the patient receiving chemotherapy in association with PBSCT Visible oral disease Significantly reduced platelet and neutrophil count

Sites / Locations

  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Placebo Comparator

Arm Label

1

2

3

4

Arm Description

ATL-104 50mg

ATL-104 100mg

ATL-104 150mg

Placebo

Outcomes

Primary Outcome Measures

Safety: Adverse events
Efficacy: Oral mucositis scale

Secondary Outcome Measures

Safety: Laboratory monitoring, vital signs, ECG
Pharmacokinetics of ATL-104

Full Information

First Posted
September 9, 2005
Last Updated
February 11, 2008
Sponsor
Alizyme
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1. Study Identification

Unique Protocol Identification Number
NCT00163280
Brief Title
Safety, Tolerability and Efficacy of ATL-104 in Oral Mucositis
Official Title
Randomised Double-Blind Placebo-Controlled Study of Orally Administered ATL-104 to Assess Safety, Tolerance and Effect on Oral Mucositis in Patients Following Treatment With Chemotherapy and Peripheral Blood Stem Cell Transplant (PBSCT)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2008
Overall Recruitment Status
Completed
Study Start Date
July 2004 (undefined)
Primary Completion Date
December 2005 (Actual)
Study Completion Date
December 2005 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Alizyme

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This purpose of this study is to investigate whether ATL-104 is safe and well tolerated, and whether it shows evidence of efficacy in mucositis in patients undergoing PBSCT
Detailed Description
Mucositis is a serious side effect of cancer therapy and Peripheral Blood Stem Cell Transplant (PBSCT) which requires appropriate and effective management. Mucositis is a condition in which there is inflammation and ulceration of the mouth, throat and gut caused by damage to the mucosal barrier induced by chemo- and radiotherapy. Symptoms include pain, nausea, abdominal cramping, and vomiting. This study will investigate whether ATL-104, when administered as a swallowable mouthwash, is safe and well tolerated in patients undergoing PBSCT and to investigate its potential to reduce the level of severity of mucositis associated with PBSCT.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mucositis
Keywords
Mucositis, Peripheral blood stem cell transplant

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
63 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
ATL-104 50mg
Arm Title
2
Arm Type
Experimental
Arm Description
ATL-104 100mg
Arm Title
3
Arm Type
Experimental
Arm Description
ATL-104 150mg
Arm Title
4
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Drug
Intervention Name(s)
ATL-104
Intervention Description
Daily does of ATL-104 (50,100 or 150mg) or placebo for 3 days prior to the start of chemotherapy and peripheral blood stem cell transplantation. Following stem cell transplantation patients received 3 further daily doses of ATL-104 (50, 100 or 150mg) or placebo.
Primary Outcome Measure Information:
Title
Safety: Adverse events
Time Frame
28 days post-treatment
Title
Efficacy: Oral mucositis scale
Time Frame
28 days post-treatment
Secondary Outcome Measure Information:
Title
Safety: Laboratory monitoring, vital signs, ECG
Time Frame
28 days post-treatment
Title
Pharmacokinetics of ATL-104

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with haematological malignancies undergoing chemotherapy in association with PBSCT Exclusion Criteria: Clinically significant conditions that would exclude the patient receiving chemotherapy in association with PBSCT Visible oral disease Significantly reduced platelet and neutrophil count
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert Marcus
Organizational Affiliation
Addenbrooke's Hospital, Cambridge, UK
Official's Role
Principal Investigator
Facility Information:
Facility Name
Research Site
City
Birmingham
Country
United Kingdom
Facility Name
Research Site
City
Cambridge
Country
United Kingdom
Facility Name
Research Site
City
Cardiff
Country
United Kingdom
Facility Name
Research Site
City
Leeds
Country
United Kingdom
Facility Name
Research Site
City
Leicester
Country
United Kingdom
Facility Name
Research Site
City
London
Country
United Kingdom
Facility Name
Research Site
City
Oxford
Country
United Kingdom
Facility Name
Research Site
City
Plymouth
Country
United Kingdom

12. IPD Sharing Statement

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Safety, Tolerability and Efficacy of ATL-104 in Oral Mucositis

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