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CompletedNCT00367016XolairUpdated Jul 13, 2021Results posted

Immunologic Basis of Anti-IgE Therapy (Study II: On Patients With Asthma)

A Phase 4 interventional study of Omalizumab and Placebo in Asthma, Allergic Rhinitis and Atopic Dermatitis, sponsored by University of California, Davis. Completed at 1 site in United States. Open to participants aged 18 Years to 55 Years. Per ClinicalTrials.gov, last updated 2021-07-13.

Sponsored by University of California, Davis · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
6
Allocation
Randomized
Ages
18 Years to 55 Years
Sex
All
01

Study summary

The purpose of this study is to look at measures that will help scientists understand the way Omalizumab, an FDA-approved anti-allergy medication, works.

Read the detailed description

IgE is a key molecule involved in immediate hypersensitivity and plays a major role in the pathogenesis of allergic diseases. Recently, a therapy based on the use of anti-IgE antibody has been developed by a pharmaceutical company, Genentech. A number of clinical trials have demonstrated that these antibodies are efficacious in treatment of allergies, including allergic rhinitis and asthma. The medication Omalizumab (Xolair) has recently been approved by the FDA for treatment of asthma.

The mechanism underlying the beneficial effect of this therapy is not completely understood, but is likely to be related to the marked reduction in the IgE level. Of note is the concomitant accumulation of IgE-anti-IgE complexes in the sera. Another remarkable effect of the treatment is the substantial reduction in the FcεRI level on basophils, which is likely a key factor contributing to the therapeutic benefit of the drug. The existing literature suggests that the reduction in the IgE level is likely to result in a down-regulation of another IgE receptor, FcεRII/CD23. Because of the known immunomodulatory function of FcεRII, anti-IgE therapy may result in alterations of the immune system, in addition to simple absorption of IgE.

We propose to conduct mechanistic studies of anti-IgE therapy. The objectives are to address how anti-IgE therapy works and how it might affect the immune system in general. The proposed studies also take advantage of this well-defined therapy to address some basic questions regarding the immune system. Our hypothesis is that anti-IgE therapy may have general effects on the immune system, such as reduced IgE-mediated antigen presentation by antigen-presenting cells and suppressed allergen-specific IgE and IgG production. The specific aims of the proposed research are:

  1. Determination of the effect of anti-IgE therapy on FcεRI expression and basophil responses. We will first confirm that anti-IgE therapy causes a reduction in the FcεRI level on basophils and then analyze whether this occurs at a transcriptional level. We will confirm that the therapy causes a reduction in basophil response to cross-linkage of FcεRI and then determine whether it also affects basophil response induced by non-IgE stimuli. The effect of the therapy on the FcεRI level on skin mast cells will also be investigated.
  2. Determination of the effect of anti-IgE therapy on FcεRII expression and antigen presentation. We will determine whether the therapy results in a down-regulation of FcεRII/CD23 on B cells. Because of the demonstrated function of FcεRII/CD23 in antigen presentation, we will determine the antigen presentation to T cells by B cells from anti-IgE-treated and control subjects.
  3. Determination of the effect of anti-IgE therapy on antibody production. We will determine whether anti-IgE therapy results in a suppression of IgE production, in addition to sequestration of IgE. Whether IgE-anti-IgE complexes directly suppress IgE production by B cells in vitro will be investigated.
02

Conditions studied

  • Asthma
  • Allergic Rhinitis
  • Atopic Dermatitis
03

In context

Rhinitis

1,105 studies on the registry are indexed under Rhinitis; 65 are open to participants now.

This study's enrollment of 6 is below the median of 89 across 906 interventional studies indexed under Rhinitis.

Browse Rhinitis studies →

Lead sponsor

University of California, Davis is the lead sponsor of 798 studies on the registry; 146 are open to participants now.

Of its 65 completed or terminated interventional studies of FDA-regulated products, 43 (66%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Mild or moderate persistent asthma
  • Allergic rhinitis
  • Atopic dermatitis

Exclusion criteria

Exclusion Criteria:

  • Other lung diseases
  • Blood clotting disorder
  • Pregnant or lactating women
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Double (Participant, Investigator)
Enrollment
6 participants (actual)

Study arms

  • Experimental
    Omalizumab

    Subjects will receive subcutaneous Omalizumab for 6 months. Prior to Omalizumab administration, all subjects will undergo screening studies, including spirometry, blood test and skin test. Blood test includes comprehensive metabolic panel, CBC, and total and free IgE levels. Skin test will be done with a panel of 7 common allergens

    Drug: Omalizumab

  • Experimental
    Placebo

    Subjects will receive subcutaneous placebo for 6 months. Prior to placebo administration, all subjects will undergo screening studies, including spirometry, blood test and skin test. Blood test includes comprehensive metabolic panel, CBC, and total and free IgE levels. Skin test will be done with a panel of 7 common allergens

    Drug: Placebo

Interventions

  • DrugOmalizumab

    Xolair (Omalizumab) will be given by subcutaneous injection according to Ige level and weight calculation.

    Also known as: Xolair

  • DrugPlacebo

    Placebo, given by subcutaneous injection.

06

What researchers measure

Primary outcomes

  1. FcεRI (High Affinity Receptor) Levels at 3 Months

    Skin biopsies were collected from patients after 0 (pre), 3 (pos1) and 6 (pos2) months of omalizumab (P11, P36, P42) or placebo (P7 and P38) treatment. The skin was fixed and the paraffin-embedded sections were stained for high affinity receptors. The average numbers of positively stained cells in each field were counted under a microscope at 400X magnification.

    Time frame: 3 months

  2. FcεRI (High Affinity Receptor) Levels at 6 Months

    Skin biopsies were collected from patients after 0 (pre), 3 (pos1) and 6 (pos2) months of omalizumab (P11, P36, P42) or placebo (P7 and P38) treatment. The skin was fixed and the paraffin-embedded sections were stained for high affinity receptors. The average numbers of positively stained cells in each field were counted under a microscope at 400X magnification.

    Time frame: 6 months

Secondary outcomes

  1. Total Sera IgE Levels at 6 Months

    Total sera IgE levels are increased upon anti-IgE treatment. Sera from each patient were collected every month after omalizumab (P11, P36 and P42) or placebo (P7, P37 and P38) treatment. The sera IgE levels were measured by ELISA using polyclonal goat anti-human IgE as the capture antibody and HRP-goat anti-human IgE as the detection antibody.

    Time frame: 6 months

07

Results

Posted Jul 13, 2021
Limitations and caveats
There are no limitations and caveats.

Participant flow

Participant flow — Overall Study
MilestoneOmalizumabPlacebo
Started33
First intervention33
Second intervention33
Completed33
Not completed00

Outcome measures

PrimaryFcεRI (High Affinity Receptor) Levels at 3 Months

Skin biopsies were collected from patients after 0 (pre), 3 (pos1) and 6 (pos2) months of omalizumab (P11, P36, P42) or placebo (P7 and P38) treatment. The skin was fixed and the paraffin-embedded sections were stained for high affinity receptors. The average numbers of positively stained cells in each field were counted under a microscope at 400X magnification.

Time frame:
3 months
Reported as:
Mean · Positive cells per field
FcεRI (High Affinity Receptor) Levels at 3 Months
Positive cells per fieldOmalizumabPlacebo
FcεRI (High Affinity Receptor) Levels at 3 Months20.5 (3 to 38)13.66 (8 to 28)
PrimaryFcεRI (High Affinity Receptor) Levels at 6 Months

Skin biopsies were collected from patients after 0 (pre), 3 (pos1) and 6 (pos2) months of omalizumab (P11, P36, P42) or placebo (P7 and P38) treatment. The skin was fixed and the paraffin-embedded sections were stained for high affinity receptors. The average numbers of positively stained cells in each field were counted under a microscope at 400X magnification.

Time frame:
6 months
Reported as:
Mean · Positive cells per field
FcεRI (High Affinity Receptor) Levels at 6 Months
Positive cells per fieldOmalizumabPlacebo
FcεRI (High Affinity Receptor) Levels at 6 Months17 (5 to 38)22.5 (15 to 30)
SecondaryTotal Sera IgE Levels at 6 Months

Total sera IgE levels are increased upon anti-IgE treatment. Sera from each patient were collected every month after omalizumab (P11, P36 and P42) or placebo (P7, P37 and P38) treatment. The sera IgE levels were measured by ELISA using polyclonal goat anti-human IgE as the capture antibody and HRP-goat anti-human IgE as the detection antibody.

Time frame:
6 months
Reported as:
Mean · U/ml
Total Sera IgE Levels at 6 Months
U/mlOmalizumabPlacebo
Total Sera IgE Levels at 6 Months300 (0 to 600)883.33 (300 to 1200)

Adverse events

Collected over 12 months. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Omalizumab0/3 (0%)0/3 (0%)0/3 (0%)
Placebo0/3 (0%)0/3 (0%)0/3 (0%)

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)OmalizumabPlaceboTotal
<=18 years000
Between 18 and 65 years235
>=65 years101
Sex: Female, Male
Sex: Female, Male(Participants)OmalizumabPlaceboTotal
Female213
Male123
08

Study locations

1 site
  • UC Davis Department of Dermatology
    Sacramento, California 95816, United States
09

References and documents

10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 13, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT00367016
Lead sponsor
University of California, Davis
Responsible party
Sponsor
First posted
Aug 22, 2006
Start date
Feb 2004
Primary completion
Oct 17, 2012
Completion
Oct 17, 2012
Results posted
Jul 13, 2021
Last update
Jul 13, 2021

Study contacts

Fu-Tong Liu, M.D., Ph.D.
principal investigator · University of California, Davis

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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