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Completed

NCT Number: NCT02797847

A Safety and Tolerability Study of an Investigational Drug, ALN-TTRSC02, in Healthy Subjects

The purpose of this study is to determine the safety, tolerability, pharmacokinetics and pharmacodynamics of ALN-TTRSC02 in healthy subjects.

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Key information

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Male and female subjects, age 18 to 65 years, inclusive.
  • Body mass index (BMI) ≥18.0 kg/m2 and ≤30 kg/m2 assessed at Screening.
  • No clinically significant health concerns, as determined by medical history and physical examination, in the opinion of the Investigator.
  • Women of child bearing potential must have a negative pregnancy test, cannot be breastfeeding, and must be willing to use contraception, willing and able to comply with the study requirements and to provide written informed consent.
  • For Japanese cohorts, subjects of Japanese descent are defined as people carrying a Japanese passport, descendants of 4 Japanese grandparents, and have not been outside Japan for more than 5 years.

Exclusion criteria

  • Clinically relevant history or presence of respiratory, gastrointestinal, renal, cardiovascular, hepatic, hematological, lymphatic, neurological, psychiatric, musculoskeletal, genitourinary, immunological, and other inflammatory diseases, or dermatological or connective tissue diseases or disorders.
  • Active serious mental illness or psychiatric disorder.
  • Clinically significant ECG abnormalities. Abnormal for AST/ALT and any other clinical safety laboratory result considered clinically significant.
  • Known history of allergic reaction to an oligonucleotide or GalNAc.
  • History of intolerance to subcutaneous injection.

Treatment and study plan

ALN-TTRSC02

Drug

Ascending doses of ALN-TTRSC02 by subcutaneous (SC) injection

Sterile Normal Saline (0.9% NaCl)

Drug

Calculated volume to match active comparator

Primary outcomes

  1. Safety of ALN-TTRSC02, evaluated by the proportion of subjects experiencing adverse events (AEs)

    Time frame: Day 1 through to Day 314

Secondary outcomes

  1. Profile of pharmacokinetics (PK) of ALN-TTRSC02

    Time frame: Day 1 through to Day 3

    Cmax

  2. Profile of pharmacokinetics (PK) of ALN-TTRSC02

    Time frame: Day 1 through to Day 3

    tmax

  3. Profile of pharmacokinetics (PK) of ALN-TTRSC02

    Time frame: Day 1 through to Day 3

    AUC

  4. Profile of pharmacokinetics (PK) of ALN-TTRSC02

    Time frame: Day 1 through to Day 3

  5. Profile of pharmacokinetics (PK) of ALN-TTRSC02

    Time frame: Day 1 through to Day 3

    CL/F

  6. Profile of pharmacokinetics (PK) of ALN-TTRSC02

    Time frame: Day 1 through to Day 3

    Vss/F

  7. Profile of pharmacokinetics (PK) of ALN-TTRSC02

    Time frame: Day 1 through to Day 3

    Vz/F

  8. Profile of pharmacokinetics (PK) of ALN-TTRSC02

    Time frame: Day 1 through to Day 314

    fe

  9. Profile of pharmacokinetics (PK) of ALN-TTRSC02

    Time frame: Day 1 through to Day 314

    CLR

  10. Effect of ALN-TTRSC02 on serum TTR levels as measured by reduction from baseline in serum TTR

    Time frame: Day 1 through to Day 314

  11. Effect of ALN-TTRSC02 on serum Vitamin A levels as measured by reduction from baseline in serum Vitamin A

    Time frame: Screening through to Day 314

Sponsors and collaborators

Lead sponsor

Alnylam Pharmaceuticals

Industry

Registry information

Official study title

A Phase 1, Randomized, Single-Blind, Placebo Controlled, Single-Ascending Dose, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics Study of Subcutaneously Administered ALN-TTRSC02 in Healthy Subjects

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Jun 14, 2016
Registry last updated
Sep 21, 2018

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.

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