North American Study of Epistaxis in Hereditary Hemorrhagic Telangiectasia (HHT)

Phase 2

Completed

• Conditions: Telangiectasia, Hereditary Hemorrhagic; Epistaxis
• Interventions: Drug: Sterile saline; Drug: Estriol; Drug: Bevacizumab; Drug: Tranexamic Acid

• Registration Number: NCT01408030
• Lead Sponsor: James Gossage

Brief Summary

The purpose of the NOSE Study is to carefully examine the efficacy and safety of 3 nasal sprays (bevacizumab, estriol, and tranexamic acid), compared to placebo, for the treatment of HHT related nosebleeds.

Detailed Description

140 patients with moderate to severe epistaxis secondary to HHT will be randomized to receive one of four intranasal sprays for a period of 12 weeks and then followed for an additional 12 weeks off therapy. Enrollment will occur over a period of 18-36 months. The primary endpoint will be the frequency of epistaxis. Secondary endpoints will include duration of epistaxis, the Hoag Epistaxis Severity Score (ESS), a quality of life survey, satisfaction with treatment, hemoglobin and ferritin levels, transfusion requirements, and treatment failure. The sprays will be: saline spray (Placebo); estriol 0.1% in methylcellulose suspension (EST); tranexamic acid 10% in saline (TA), and bevacizumab 1% in saline (BEV). All sprays will be applied to the nasal mucosa by an identical spray bottle at a dose of 0.1 ml per nostril twice daily (total dose of 0.4 ml daily). Thus, the delivered doses will be: EST, 0.4 mg/day; TA, 40 mg/day; BEV, 4 mg/day.

Study Timeline

• Study Start: 2011-08
• Study First Submitted: 2011-08-01
• Study First Submitted QC: 2011-08-01
• Study First Posted: 2011-08-02
• Primary Completion: 2014-09
• Study Completion: 2014-09
• Results First Submitted: 2018-09-11
• Status Verified: 2018-10
• Results First Submitted QC: 2018-10-09
• Last Update Submitted: 2018-10-09
• Results First Posted: 2018-10-19
• Last Update Posted: 2018-10-19

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 123

Inclusion Criteria

1. A diagnosis of definite or possible HHT by the Curacao criteria (Shovlin 2000) or a positive DNA test for HHT (as characterized by a disease causing mutation in the gene coding for endoglin, activin like kinase 1, or SMAD-4). According to the Curacao criteria, a definite diagnosis of HHT is defined as having at least 3 of the following criteria while a possible diagnosis is defined as 2 criteria:

   1. Spontaneous and recurrent epistaxis.
   2. Multiple telangiectasias at characteristic sites (lips, oral cavity, fingers, nose).
   3. Visceral lesions such as gastrointestinal telangiectasias and arteriovenous malformations (AVM) in lung, brain, spine and liver.
   4. A history of definite HHT in a first degree relative using these same criteria.

2. Epistaxis of at least 1 minute (on average) and which occurs at least once weekly when averaged during the preceding 8 weeks.

3. Epistaxis severity score (ESS) of at least 3.0.

4. Age of at least 18 years.

5. Written and informed consent obtained prior to study entry.

6. Subject is able and willing to return for outpatient visits.

7. The epistaxis is considered to be clinically stable during the past 8 weeks in the clinical judgment of the investigator (i.e. no major changes in frequency or duration of epistaxis or in transfusion requirements).

8. Negative pregnancy test at enrollment.

Exclusion Criteria

1. Allergy to any of the active treatment agents or their spray additives.

2. Estimated life expectancy less than 1 year.

3. A psychiatric or substance abuse problem that is expected to interfere with study compliance.

4. History of deep venous thrombosis (DVT), pulmonary embolism (PE), acute myocardial infarction (MI), arterial thromboembolism, or ischemic stroke in the past 6 months.6. History of receiving more than 12 units of red blood cells in the past 12 weeks.

5. Presence of an untreated coagulopathy that is felt to be contributing to the 5. History of estrogen receptor positive breast cancer. epistaxis. 8. Presence of active disseminated intravascular coagulation. 9. Uncontrolled hypertension (systolic BP >160 and/or diastolic BP >100). 10. Presence of untreated brain AVM. 11. Presence of active malignancy in the brain, lung, or colon. 12. Presence of symptomatic heart failure. 13. Use of estrogens, epsilon aminocaproic acid, tranexamic acid, or thalidomide by any route for more than 1 week in the past 12 weeks. Any use of a VEGF inhibitor by any route in the past 24 weeks.

6. Baseline use of the following anticoagulants is not allowed: warfarin or other vitamin K antagonists at any dose; unfractionated or low molecular weight heparins at standard doses for treatment of venous thromboembolism (VTE); or aspirin at >325 mg/day. Baseline use of the following anticoagulants is allowed: heparins at standard doses for VTE prophylaxis; clopidogrel; or aspirin at ≤325 mg/day.

7. Addition of new treatments for epistaxis in the past 12 weeks (including laser ablation of nasal telangiectasias and over the counter medications).

8. Presence of another overt cause (e.g. overt gastrointestinal bleeding) that is felt to be significantly contributing to anemia.

9. Lactating women.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Placebo spray	Sterile saline	sterile saline
Estriol spray	Estriol	Estriol 0.1%
Bevacizumab spray	Bevacizumab	bevacizumab 1%
Tranexamic acid spray	Tranexamic Acid	tranexamic acid 10%

Primary Outcome Measures

Name	Time	Method
Frequency of Epistaxis	Weeks 5-12 of active treatment phase	Bleeding episodes per week

Secondary Outcome Measures

Name	Time	Method
Hoag Epistaxis Severity Score	12 weeks	Hoag Epistaxis Severity Score (ESS) is based on 6 nosebleed variables such as frequency and duration which are entered by patients. The ESS has a minimum value of 0 and maximum value of 10, with 10 representing more severe epistaxis.
Duration of Epistaxis	5-12 weeks of active treatment	Total minutes of bleeding per week
Hemoglobin Level	12 weeks	grams/100 ml, assessed at week 12
Number of Participants Requiring Red Blood Cell (RBC) Transfusion	12 weeks	Number of participants requiring RBC transfusion during weeks 1-12
Number of Participants With Treatment Failure	Baseline through 12 weeks	Treatment failure is defined as the occurrence of one or more of the following during the study: need for nasal surgery or chemical cautery or other new treatment modality to control epistaxis; transfusion of more than 12 units of RBC; severe complications such as acute myocardial infarction, venous thromboembolism, brain hemorrhage; or death

Trial Locations

Locations (6)

University of California Los Angeles; 🇺🇸 Los Angeles, California, United States

Georgia Regents University; 🇺🇸 Augusta, Georgia, United States

University of Utah; 🇺🇸 Salt Lake City, Utah, United States

Oregon Health Sciences University; 🇺🇸 Portland, Oregon, United States

Washington University School of Medicine; 🇺🇸 Saint Louis, Missouri, United States

Johns Hopkins University; 🇺🇸 Baltimore, Maryland, United States