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Phase 1 N=44 Randomized Double-blind Basic Science

Safety and Tolerability of MEDI9314 as Single Ascending Dose in Healthy Subjects

Safety · Healthy Subjects

Enrolled (actual)
44
Serious AEs
0.0%
Results posted
May 2019
Primary outcome: Primary: Number of Participants With Treatment-emergent Adverse Events (TEAEs) and Treatment-emergent Serious Adverse Events (TESAEs) — 8; 4; 2; 5 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 1
Interventions
MEDI9314 (Drug); placebo (Drug)
Age
Adult · 18+ yrs
Sex
All
Sponsor
MedImmune LLC
Primary completion
Nov 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Treatment-emergent Adverse Events (TEAEs) and Treatment-emergent Serious Adverse Events (TESAEs)
8; 4; 2; 5; 4; 5
PRIMARY
Number of Participants With Electrocardiogram Abnormalities Reported as TEAEs
0; 0; 0; 0; 0; 0
PRIMARY
Number of Participants With Vital Signs Abnormalities Reported as TEAEs
0; 0; 0; 1; 0; 0
PRIMARY
Number of Participants With Physical Examination Abnormalities Reported as TEAEs
0; 0; 0; 0; 0; 0
PRIMARY
Number of Participants With Clinical Laboratory Abnormalities Reported as TEAEs
0; 0; 0; 0; 1; 0
PRIMARY
Number of Participants With TEAEs Related to Injection Site Reactions
0; 0; 0; 0; 0; 1
SECONDARY
Area Under the Serum Drug Concentration Versus Time Curves From Zero to Infinity (AUC 0-inf) of MEDI9314
3.01; 68.8; 179; 264; 668; 1440
SECONDARY
Area Under the Serum Drug Concentration Versus Time Curve, to Last Quantifiable Time Point (AUClast)
2.94; 68.6; 178; 264; 667; 1439
SECONDARY
Maximum Observed Serum Drug Concentration (Cmax) of MEDI9314
0.425; 5.44; 10.4; 14.1; 79.0; 108
SECONDARY
Time to Maximum Observed Serum Drug Concentration (Tmax) of MEDI9314
4.00; 8.07; 5.52; 5.51; 0.04; 0.04
SECONDARY
Terminal Phase Elimination Half-life (t1/2) of MEDI9314
1.74; 3.55; 4.72; 5.03; 7.31; 8.95
SECONDARY
Serum Concentrations of MEDI9314
21.495; 9.770; 22.577; 9.770; 9.770; 9.770
SECONDARY
Number of Participants Positive for Anti-Drug Antibodies to MEDI9314
0; 0; 0; 0; 0; 1

Summary

This is a phase 1a randomized, blinded, placebo-controlled, single-ascending dose study to assess the safety and tolerability of MEDI9314 in healthy adult subjects

Eligibility Criteria

Inclusion Criteria

  • Written informed consent.
  • Age 18 through 50 years at the time of screening.
  • Female subjects must be of non-childbearing potential.
  • Nonsterilized males who are sexually active with a female partner of childbearing potential must use condom and spermicide.
  • Body mass index of 19.0 through 32.0 kg/m2 at screening.
  • No clinically significant abnormality on the basis of medical/medication history or physical examination.
  • Negative drugs of abuse (DOA).
  • Able and willing to comply with the requirements of the protocol and complete the study until the end of the safety follow up period.
  • For the Japanese Cohort, both of the subject's parents and both sets of grandparents must be Japanese.

Exclusion Criteria

  • Any condition that, in the opinion of the investigator, would interfere with evaluation of the investigational product or interpretation of subject safety or study results.
  • Concurrent enrollment in another clinical study involving any treatment.
  • Individuals who are legally institutionalized.
  • Receipt of > 2 marketed or investigational biologic agents.
  • Receipt of an investigational biologic agent within 4 months or 5 half-lives prior to screening, whichever is longer.
  • Receipt of any investigational non biologic agent within 3 months or 5 half lives prior to screening, whichever is longer.
  • Use of any medication (prescription or over the counter, including herbal remedies) within 14 days or 5 half lives of Day 1, whichever is longer, unless in the opinion of the investigator and medical monitor the medication will not interfere with the study procedures or compromise subject safety.
  • Known history of allergy or reaction to any component of the investigational product formulation.
  • History of anaphylaxis following any biologic therapy.
  • Any clinically relevant abnormal findings in physical examination ECG, vital signs, and laboratory parameters.
  • Positive tuberculosis (TB) test (QuantiFERON®-TB Gold In-tube).
  • Positive hepatitis B surface antigen, hepatitis C virus antibody or HIV test at screening.
  • Receipt of live attenuated vaccines 30 days prior to the date of screening.
  • Where donation of blood or blood products was in excess of 500 mL within an 8-week period in the 3 months prior to screening.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02669667). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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