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Efficacy and Safety Study of TOLAMBA™ in Ragweed-Allergic Adults

A Randomized, Double-Masked, Placebo-Controlled, Multicenter, Dose-Regimen Study of the Efficacy and Safety of TOLAMBA™ in Ragweed-Allergic Rhinitis Adults

Status
Terminated
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00387738
Enrollment
738
Registered
2006-10-13
Start date
2006-04-30
Completion date
2008-03-31
Last updated
2019-04-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rhinitis, Allergic, Seasonal

Keywords

Ragweed, Allergy, Allergic, Rhinitis, Hay Fever, Seasonal, Treatment, Immunotherapy, Vaccine

Brief summary

The purpose of this study is to find out if a new investigational vaccine, TOLAMBA™, is safe and effective in reducing the symptoms of ragweed allergy.

Detailed description

Ragweed allergy is the most common seasonal allergy in North America. Allergen immunotherapy is a therapeutic option for patients who have allergy symptoms that cannot be adequately controlled by avoidance of the allergen or medication. It may also be appropriate for those who cannot tolerate their medications due to side effects or have difficulties with medication compliance. This study compares the safety and efficacy of two different dosing regimens of TOLAMBA™ with placebo in reducing the symptoms of ragweed-allergic adults over two consecutive ragweed pollen seasons. Comparison(s): Subject-rated allergy symptoms of subjects treated with TOLAMBA™ dose-intense regimen or TOLAMBA™ lower-dose regimen, compared with subjects treated with placebo.

Interventions

BIOLOGICALAmb a 1 immunostimulatory oligodeoxyribonucleotide conjugate

Escalating doses, 6 weekly subcutaneous (under the skin) injections

BIOLOGICALHistamine base

Escalating doses, 6 weekly subcutaneous (under the skin) injections

Sponsors

Dynavax Technologies Corporation
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Has a history of ragweed allergic rhinitis (hayfever) during at least the last 2 consecutive seasons that has required treatment with antihistamines, decongestants and/or nasal steroids, but where symptom relief has been incomplete * Is willing to stay in their ragweed area during the historical peak period of the local ragweed season, and willing to travel for no more than 2 weeks (cumulative time) outside of their ragweed area during the entire season

Exclusion criteria

* Has had any hospital admissions for asthma * Has smoked within the past year, or has a ≥10-pack per year smoking history * Has had any previous immunotherapy with ragweed pollen extract, or was in a previous clinical trial with TOLAMBA™ * Has used Xolair within the past 12 months * Has a history of anaphylaxis

Design outcomes

Primary

MeasureTime frame
Change from baseline in total nasal symptom score during the peak period of the ragweed pollen season.Two years

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026