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OpenTrials
Completed

NCT Number: NCT04146129

A Phase 1 Study of CDX-0159

This is a study to determine the safety of CDX-0159 in healthy subjects.

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Key information

Conditions

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Altasciences Clinical Kansas, Inc.

Overland Park, Kansas, 66212, United States

About this study

CDX-0159 is a humanized monoclonal antibody that binds to a protein called KIT that is expressed on mast cells.

This study will evaluate the safety, pharmacokinetics, and pharmacodynamics of CDX-0159 in healthy subjects.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Key Inclusion Criteria:

  • An informed consent signed and dated by the subject.
  • Healthy volunteer aged 18-55.
  • In generally good health and without significant medical conditions based on physical exam, ECG, and laboratory test results.
  • Body mass index (BMI) ≥ 18.5 kg/m2 to ≤ 30 kg/m2
  • No medication other than mild analgesics, vitamins and mineral supplements or, oral contraceptives
  • Both males and females of child bearing potential must agree to use a medically accepted contraceptive regimen during study and up to 150 days afterwards.
  • Not a current smoker (or regular user of any nicotine containing product).
  • Willing to follow all study rules

Key Exclusion Criteria:

  • Women who are pregnant or nursing
  • History of anaphylaxis, food allergies, or allergies (chronic or seasonal) requiring prescription medication
  • Autoimmune disorders requiring more than topical medication
  • History of asthma requiring the use of inhaled medication within the past 5 years.
  • Vaccination with live vaccines within 4 weeks prior to study drug administration (subjects must agree to avoid vaccination during the study).
  • Positive urine test for alcohol and drugs of abuse.

Other Protocol defined inclusion and exclusion criteria could apply.

Treatment and study plan

CDX-0159

Drug

Single dose of one of four dosages of CDX-0159

normal saline

Drug

Single infusion of normal saline

Primary outcomes

  1. Safety as assessed by CTCAE v5.0

    Time frame: Day 1 to Day 43.

    Safety of single, ascending doses of CDX-0159 as determined by percentage of participants with adverse events as assessed by CTCAE v5.0.

Sponsors and collaborators

Lead sponsor

Celldex Therapeutics

Industry

Registry information

Official study title

A Randomized, Double-Blind, Placebo-Controlled, Phase 1 Single Ascending Dose Study to Assess the Safety, Pharmacokinetics, and Pharmacodynamics of CDX-0159 in Healthy Subjects

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Oct 31, 2019
Registry last updated
Jul 7, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.