Safety, Tolerability, Pharmacodynamic Effects and Preliminary Evidence for Efficacy of the Anti-Hypertension Vaccine CYT006-AngQb

Essential Hypertension Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00500786
• Other study ID #: CYT006-AngQb 01
• Status: Completed
• Phase: Phase 1/Phase 2
• First received: July 12, 2007
• Last updated: August 20, 2012
• Start date: November 2004
• Est. completion date: April 2007

Study information

• Verified date: August 2012
• Source: Cytos Biotechnology AG
• Contact: n/a
• Is FDA regulated: No
• Health authority: Germany: Paul-Ehrlich-Institut
• Study type: Interventional

Clinical Trial Summary

This is a multi-center, randomized, placebo-controlled, time-lagged, parallel-group study in healthy and hypertensive subjects to evaluate safety and tolerability of the vaccine CYT006-AngQb. The trial is double-blind for active vs. placebo within each treatment arm, but open with respect to AngQb dose escalation.

In the first arm, 16 healthy normotensive volunteers are treated with a one dose regimen consisting of a single s.c. injection of 100µg of AngQb or placebo. Upon satisfying safety and tolerability profile, as judged by the independent safety monitoring board, arm two is enrolled.

In arm two 36 patients with mild to moderate hypertension receive three s.c. injections of 100µg CYT006-AngQb (24 patients) or placebo (12 patients). The second and third injections are given 4 and 12 weeks after the first injection, respectively. Upon satisfying safety and tolerability profile, as judged by the independent safety monitoring board, arm three is enrolled.

In arm three 36 patients with mild to moderate hypertension receive three s.c. injections of 300µg CYT006-AngQb (24 patients) or placebo (12 patients). The second and third injections are given 4 and 12 weeks after the first injection, respectively.

The primary objective of the trial is to evaluate safety / tolerability of 3 dose regimens of CYT006-AngQb in healthy volunteers and patients with mild to moderate essential hypertension. Secondary objectives include the assessment of pharmacodynamic effects and their dose-response (immunogenicity and biomarkers of the renin-angiotensin system), and the exploration of clinical efficacy (effects on systolic and diastolic blood pressure)

Recruitment information / eligibility

• Status: Completed
• Enrollment: 88
• Est. completion date: April 2007
• Est. primary completion date: September 2006
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Patients with untreated mild-to-moderate essential hypertension, clinically diagnosed according to the World Health Organization criteria (systolic blood pressure =140-179 mm Hg and/or diastolic blood pressure =90-109 mm Hg on 3 consecutive occasions; standardized after 5 minutes in sitting position)

• Patients with newly diagnosed essential hypertension or previously treated patients from whom antihypertensive therapy can be safely withdrawn for the duration of the study.

• 18 to 65 years of age, males and non-reproductive females (surgically sterilized or post-menopausal)

• Written informed consent

• Patient is willing and able to comply with all trial requirements

Exclusion Criteria:

• Secondary hypertension

• Severe essential hypertension

• Current pharmacological treatment that could affect blood pressure

• Significant renal insufficiency [Serum creatinine > 159 µmol/L (> 1.8 mg/dl)]

• History of cerebrovascular disease

• Type 1 Diabetes or poorly controlled Type 2 Diabetes

• Body mass index (BMI) >32

• Total cholesterol > 6.9 mmol/L (> 266 mg/dl)

• Triglycerides > 3.5 mmol/L ( > 174.3 mg/dl)

• Autoimmune diseases or severe allergies

• Patients with a history of HIV infection, AIDS, hepatitis B or C, or other immunosuppressive disorders

• Current diagnosis or a history of malignancy

• Drug or alcohol abuse within the past 2 years

• Pregnancy or breastfeeding

• Present history of mental diseases

• Participation in any drug trial within three month of onset of current trial

• Previous participation in a clinical trial with a Qb based vaccine (DerQb, NicQb, AllQb)

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Essential Hypertension
• Hypertension

Intervention

Biological:
• CYT006-AngQb

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Cytos Biotechnology AG

External Links

•   Sponsor's web page