A Phase 1 Safety, Pharmacokinetic, and Immunologic Study to Evaluate CDX-301 (rhuFlt3L) in Healthy Volunteers
Trial Snapshot
- Phase
- Phase 1
- Status
- Completed
- Sponsor
- Celldex Therapeutics
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- Number of reported adverse events
Study Overview
Brief Summary
CDX-301 is a protein that stimulates the growth of bone marrow stem cells and certain immune cells. This study is testing CDX-301 in healthy volunteers who will be monitored for safety and biological response for approximately one month or more.
Detailed Description
A total of seven cohorts of healthy volunteers are planned with doses of CDX-301 (rhuFlt3L) ranging between 1 and 75 μg/kg and dosing durations between 5 and 10 days.
Volunteers will be admitted to an inpatient unit during the Treatment Period. Blood samples will be collected periodically to assess the effect of CDX-301. Volunteers will be followed for safety for 28 days following the last dose. Any volunteer who develops anti-CDX-301 antibodies will be followed monthly until the antibody response is below the limit of detection. In general, the total duration of the study will be between approximately 33-38 days.
Study Design
- Study Type
- Interventional
- Allocation
- Non Randomized
- Intervention Model
- Single Group
- Primary Purpose
- Other
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 55 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Among other criteria, volunteers must meet the following conditions to be eligible for the study:
- •Ages 18 - 55
- •Body Weight ≤ 120 kg
- •Generally good health and without significant medical conditions
- •Willing to use effective method of contraception
- •Abstinence from alcohol for 72 hours prior to study drug administration and throughout the study
- •Negative screening test for HIV, hepatitis B, and hepatitis C
- •Provide written informed consent
Exclusion Criteria
- •Among other criteria, volunteers who meet the following conditions are NOT eligible for the study:
- •Drug or alcohol abuse within 12 months
- •Positive drug screen
- •Receipt of certain types of experimental drugs or other treatments, or certain medications
- •Use of systemic immunosuppressive agents (excluding topical steroids) within 12 months
- •History of certain diseases including syphilis, herpes zoster, primary or secondary immunodeficiency
- •Diagnosis with or family history of significant autoimmunity (ex: type I diabetes, multiple sclerosis, rheumatoid arthritis, scleroderma)
- •Any history of cancer, excluding adequately treated and cured basal or squamous cell carcinoma of the skin, or cervical carcinoma in situ within 2 years
- •History of asthma requiring any use of inhaled or oral medication within 5 years
- •Herpes zoster within 3 months
- •Donation of blood within 8 weeks, and donation of plasma within 2 weeks
Arms & Interventions
CDX-301
CDX-301 (rhuFlt3L), administered to healthy patients.
Intervention: CDX-301 (Drug)
Outcomes
Primary Outcomes
Number of reported adverse events
Time Frame: Until day 28 of follow up.
The number of adverse events along with the results of vital sign measurements, physical examinations, and clinical laboratory tests will be used to determine the safety profile of CDX301.
Secondary Outcomes
- Determination of PK profile of CDX301(Until day 28 of follow up or until resolution.)
- Immune system effects (eg: anti-CDX-301 antibody development, lymphoid cell populations, serum cytokines, and response to recall antigens and vaccination).(Until day 28 of follow up)