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Trial record 2 of 2 for:    AZD2820

To Assess the Safety, Tolerability and Pharmacokinetics of AZD2820 After Single Ascending Doses

This study has been completed.
Information provided by (Responsible Party):
AstraZeneca Identifier:
First received: April 6, 2011
Last updated: November 18, 2011
Last verified: November 2011
This is a randomised, single-blind, placebo-controlled Phase I study to investigate the safety, tolerability and pharmacokinetics after administration of single doses of AZD2820 to healthy male subjects.

Condition Intervention Phase
Healthy Drug: AZD2820 Drug: Placebo Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Basic Science
Official Title: A Randomised, Single-blind, Placebo-controlled Single-centre Phase I Study in Healthy Male Volunteers to Assess the Safety, Tolerability and Pharmacokinetics of AZD2820 After Single Ascending Doses

Further study details as provided by AstraZeneca:

Primary Outcome Measures:
  • Safety variables ( Adverse events, Vital signs, ECG, EEG, Regiscan, Safety labs.) [ Time Frame: Assessments performed multilpe times from the morning day 1 before dose until day 3. And then once at the follow up after 14-18 days ]

Secondary Outcome Measures:
  • To evaluate the pharmacokinetics of AZD2820 and assess the dose proportionality of the pharmacokinetics following single ascending doses of AZD2820 by assessment Cmax, tmax, t1/2 , AUC, CL/F, Ae and CLR. [ Time Frame: Blood samples will be taken multiple times from the morning day 1 before dose until day 2 ]

Enrollment: 90
Study Start Date: May 2011
Study Completion Date: November 2011
Primary Completion Date: November 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: AZD2820 Drug: AZD2820
Subcutaneous Injection in abdomen or Thigh
Placebo Comparator: Placebo Drug: Placebo
Subcutaneous Injection in abdomen or Thigh


Ages Eligible for Study:   20 Years to 45 Years   (Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Provision of signed and dated, written informed consent prior to any study specific procedures.
  • Healthy male subjects aged ≥20 - ≤45 years with suitable veins for cannulation or repeated venepuncture.
  • Male subjects should be willing to use barrier contraception ie, condoms, from the day of dosing until 3 months after dosing with the investigational product.
  • Have a body mass index (BMI) between≥ 18 and ≤30 kg/m2 and weigh at least 50 kg and no more than 100 kg.
  • Provision of signed, written and dated informed consent for genetic research. If a subject declines to participate in the genetic component of the study, there will be no penalty or loss of benefit to the subject. The subject will not be excluded from other aspects of the study described in this Clinical Study Protocol, so long as they consent.

Exclusion Criteria:

  • History of any clinically significant disease or disorder which, in the opinion of the investigator, may either put the subject at risk because of participation in the study, or influence the results or the subject's ability to participate in the study
  • History or presence of gastrointestinal, hepatic or renal disease or any other condition known to interfere with absorption, distribution, metabolism or excretion of drugs
  • A history of erectile dysfunction or anatomic abnormality of the penis (eg, cavernosal fibrosis, Peyronie's disease, or plaques) which interferes with normal erectile function
  • Predisposition or history of priapism (eg, sickle cell anemia or trait).
  • Any clinically significant illness, medical/surgical procedure or trauma within 4 weeks of the first administration of investigational product
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01332214

United Kingdom
Research Site
London, United Kingdom
Sponsors and Collaborators
Study Chair: Mirjana Kujacic, PhD AstraZeneca
Principal Investigator: Prof J Ritter BM BCh, MRCP, FRCP Quintiles, Inc.
Study Director: Mark Berner Hansen, PhD AstraZeneca
  More Information

Responsible Party: AstraZeneca Identifier: NCT01332214     History of Changes
Other Study ID Numbers: D3870C00001
Study First Received: April 6, 2011
Last Updated: November 18, 2011

Keywords provided by AstraZeneca:
Phase 1
healthy male volunteers
dose escalation
Single Ascending Dose
AZD2820 Cmax
t1/2λz processed this record on September 21, 2017