This site became the new on June 19th. Learn more.
Show more Menu IMPORTANT: Listing of a study on this site does not reflect endorsement by the National Institutes of Health. Talk with a trusted healthcare professional before volunteering for a study. Read more... Menu IMPORTANT: Talk with a trusted healthcare professional before volunteering for a study. Read more... Menu
Give us feedback
Trial record 1 of 2 for:    DSTA4637S
Previous Study | Return to List | Next Study

A Study to Investigate Safety, Tolerability, and Pharmacokinetics of DSTA4637S in Healthy Volunteers

This study has been completed.
Information provided by (Responsible Party):
Genentech, Inc. Identifier:
First received: November 3, 2015
Last updated: March 9, 2017
Last verified: March 2017
This is a Phase 1, randomized, double-blind, placebo-controlled, single-ascending dose study in healthy volunteers, enrolled at a single site in the United States to investigate the safety, tolerability, and pharmacokinetics of DSTA4637S.

Condition Intervention Phase
Healthy Volunteer Drug: DSTA4637S Drug: Placebo Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment

Further study details as provided by Genentech, Inc.:

Primary Outcome Measures:
  • Number of Participants with at least 1 Adverse Event (AE) [ Time Frame: Up to Day 85 ]

Secondary Outcome Measures:
  • Concentration of analytes of DSTA4637S in plasma and serum [ Time Frame: Up to Day 85 ]
  • Concentration of anti-therapeutic antibodies (ATA) to DSTA4637S [ Time Frame: Up to Day 85 ]

Enrollment: 30
Actual Study Start Date: November 30, 2015
Study Completion Date: May 31, 2016
Primary Completion Date: May 31, 2016 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: DSTA4637S Drug: DSTA4637S
Participants will receive DSTA4637S intravenously on Day 1.
Placebo Comparator: Placebo Drug: Placebo
Participants will receive placebo matched to DSTA4637S intravenously on Day 1.


Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Signed Informed Consent Form
  • Able to comply with the study protocol, in the investigator's judgment
  • Body mass index (BMI) between 18 and 32 kilogram per square meters (kg/m^2), inclusive
  • In good health, determined by no clinically significant findings from medical history, 12-lead electrocardiogram (ECG), and vital signs
  • Clinical laboratory evaluations should be within the reference range for the test laboratory unless deemed not clinically significant by the investigator and Sponsor
  • Willing to abstain from the use of drugs of abuse through completion of the study
  • Willing to abstain from use of over the counter, herbal or prescription medications/products from 14 days prior to Day 1 through completion of the study, unless deemed acceptable by the investigator and Sponsor
  • Agreeable to, and deemed able to (by the investigator), comply with requirements of the study, including the follow-up period
  • Willing to abstain from consumption of alcohol-based products from 72 hours prior to Day 1 until Phase 1 unit check-out on Day 3 and for 72 hours prior to each follow-up visit
  • For women of childbearing potential, agreement to remain abstinent (refrain from heterosexual intercourse) or use non-hormonal contraceptive methods that result in a failure rate of less than (<) 1 percent (%) per year during the treatment period and for at least 85 days after the last dose of study drug
  • For men, agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive measures and agreement to refrain from donating sperm, as defined in the study protocol

Exclusion Criteria:

  • Any diseases, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that in the opinion of the investigator or Sponsor contraindicates the use of an investigational drug or that may affect the interpretation of the results or render the subject at high risk from treatment complications
  • Use of tobacco, electronic cigarettes, personal vaporizer or electronic nicotine delivery systems (positive history within 3 months before initiation of dosing on Day 1)
  • Received any vaccine within 14 days prior to screening
  • Pregnant or lactating, or intending to become pregnant within 3 months after screening
  • Positive serum pregnancy test result at screening or Day &#8722;1
  • Received oral antibiotics within 4 weeks before initiation of dosing on Day 1, or intravenous antibiotics within 8 weeks before initiation of dosing
  • Hospitalization within 4 weeks before initiation of dosing
  • Positive for hepatitis C virus (HCV) antibody, hepatitis B surface antigen (HBsAg), or human immunodeficiency virus (HIV) antibody
  • History of significant drug abuse within 1 year prior to screening or use of soft drugs (such as marijuana) within 3 months prior to the screening visit or hard drugs (such as cocaine, phencyclidine, and crack) within 1 year prior to screening
  • Positive drug screen at screening or Day -1
  • History of anaphylactic or hypersensitivity drug reaction, unless approved by the investigator and Sponsor
  • Blood transfusion within 8 weeks prior to screening
  • History of malignancy within 10 years of screening except completely excised basal cell carcinoma or squamous cell carcinoma of the skin
  • Donation of plasma (greater than or equal to [>=] 500 milliliter [mL]) within 7 days prior to study drug administration
  • Donation or loss of whole blood (excluding the volume of blood that will be drawn during screening procedures) as follows: 50-499 mL of whole blood within 30 days or greater than (>) 499 mL of whole blood within 56 days prior to study drug administration
  • Hemoglobin <128 gram per liter (g/L) (males) and <115 g/L (females) and hematocrit <0.37 L/L (males) and <0.32 L/L (females) at screening
  • Poor peripheral venous access
  • History or presence of an abnormal ECG that is clinically significant in the investigator's opinion, including complete left bundle branch block, second- or third-degree heart block, evidence of prior myocardial infarction
  • Exposure to any biological therapy or investigational biological agent within 90 days prior to the screening evaluation or have received any other investigational treatment 30 days prior to the screening evaluation (or within 5 half-lives of the investigational product, whichever is greater)
  • Any history of hypersensitivity or allergy to rifampin or other rifamycin analogs
  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: NCT02596399

United States, Kansas
PRA International Clinical Pharmacology Center (EDS US Clinic)
Lenexa, Kansas, United States, 66219
Sponsors and Collaborators
Genentech, Inc.
Study Director: Clinical Trials Hoffmann-La Roche
  More Information

Responsible Party: Genentech, Inc. Identifier: NCT02596399     History of Changes
Other Study ID Numbers: GV29259
Study First Received: November 3, 2015
Last Updated: March 9, 2017

Keywords provided by Genentech, Inc.:
Healthy volunteers
DSTA4637S processed this record on September 19, 2017