Evaluation of Safety and Tolerability of Tyrosine Adsorbed Ragweed Pollen Allergoid With MPL (Monophosphoryl Lipid A)

Type I Hypersensitivity Clinical Trial

Official title:

A Double-Blind Phase I Study to Evaluate the Safety and Tolerability of Tyrosine Adsorbed Ragweed Pollen Allergoid With MPL® in Healthy Volunteers.

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT00109759
• Other study ID #: RagweedMATAMPL102
• Secondary ID: P1DP05002
• Status: Withdrawn
• Phase: Phase 1
• Start date: May 2005
• Est. completion date: June 2005

Study information

• Verified date: July 2021
• Source: Allergy Therapeutics
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The safety and tolerability of tyrosine adsorbed ragweed pollen allergoid with monophosphoryl lipid A (MPL) was planned to be evaluated. For this purpose, a total of 4 injections of either increasing doses of the study drug or placebo (tyrosine) was planned to be administered in 7-day intervals to healthy volunteers.

Description:

RagweedMATAMPL (tyrosine adsorbed ragweed pollen allergoid with monophosphoryl lipid A (MPL®)) has been developed to provide pre-seasonal specific immunotherapy for patients with proven type I hypersensitivity to ragweed pollen. MPL (Monophosphoryl Lipid A), a purified, detoxified glycolipid derived from the cell wall of Salmonella minnesota, is included in the product formulation as an adjuvant to increase the immunogenic effect of the product and to enhance the switch from an allergen-specific TH2 to a TH1-like profile.

The ragweed pollen extract is modified with glutaraldehyde to produce the active ingredient, an allergoid. This modification reduces the reactivity of the extract with IgE antibody, thus reducing the risk of side effects. However, a simultaneous reduction in other important immunological properties, such as IgG and T cell reactivities is not seen.

This was planned to be a phase I, double-blind, placebo-controlled study to evaluate the safety and tolerability of RagweedMATAMPL in healthy volunteers. Fifteen (15) volunteers were planned to be randomized to receive up to 4 subcutaneous injections of either increasing doses of RagweedMATAMPL or Placebo over 7 day intervals.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: June 2005
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• Non-smoker and not using any nicotine products

• Negative skin prick test with a standard panel of marker allergen extracts (including ragweed allergen extract)

• Specific IgE for ragweed with class = 0

• No clinical history of IgE-mediated allergic diseases

• Subject agrees not to use any medication or herbal products during the study

• Males or non-pregnant, non-lactating females who are post-menopausal, naturally or surgically sterile, or who agree to use effective contraceptive methods throughout the course of the study.

• Subjects who are normally active and otherwise judged to be in good health on the basis of medical history, physical examination, routine laboratory tests and an infection screen

• Subjects must be willing and able to attend required study visits.

• Subjects must be able to follow instructions.

Exclusion Criteria:

• Clinical history or presence of acute or subacute atopic dermatitis, chronic dermatitis, urticaria factitia, or urticaria due to physical/chemical influence.

• Clinical history or presence of diabetes, cancer or any clinically significant cardiac, respiratory, metabolic, renal, hepatic, gastrointestinal, dermatologic, venereal, hematologic, neurologic or psychiatric diseases or disorders.

• Any clinically significant (as determined by the Investigator) abnormal laboratory value at Visit 1

• Clinical history of auto-immune diseases or rheumatoid diseases.

• Contraindication to adrenaline

• History of asthma

• Subject has used any prescription medications within 14 days or over-the-counter medications, including herbal products, within 2 days prior to Screening or will likely use any medication(s) or listed product(s) during the study.

• Subject has disorder of tyrosine metabolism

• Subject with diseases with a pathogenesis interfering with the immune response and who has received medication which could influence the results of this study

• Subject has acute or chronic infection

• Clinical history of anaphylaxis

• Clinical history of angioedema

• Clinical history of hypersensitivity to the excipients of the study medication

• History of immunotherapy with ragweed allergen extracts

• Current therapy with ß-blockers

• Currently receiving anti-allergy medication or other drugs with an antihistaminic activity

• Subject has a positive screen for cotinine or drugs of abuse at Visit 1

• Subject has a positive saliva alcohol test at Visit 1

• Subject participated in a clinical trial with a new chemical substance within the last 12 months

• Subject cannot communicate reliably with the Investigator or is not likely to cooperate with the requirements of the study

• Subject is pregnant or lactating

• Clinically relevant abnormal vital signs or respiratory rate at the Screening Visit

• Subject received treatment with a preparation containing MPL® during the past 12 months.

Related Conditions & MeSH terms

• Hypersensitivity
• Hypersensitivity, Immediate
• Type I Hypersensitivity

Intervention

Biological:
• RagweedMATAMPL

Drug:
• Placebo

Locations

Country	Name	City	State
Canada	Allied Research International Inc.	Mississauga	Ontario

Sponsors (1)

Lead Sponsor	Collaborator
Allergy Therapeutics

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety and tolerability	Recording of adverse events (AEs).	29 days
Secondary	Tolerability of different subcutaneous doses	Recording of adverse events (AEs).	29 days
Secondary	Tolerability of the cumulative subcutaneous dose	Recording of adverse events (AEs).	29 days
Secondary	Clinical chemistry, hematology, respiratory rate, and ECG before and after each dose and at the end of the study		29 days