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Completed

NCT Number: NCT03651089

SP16 SERPIN-like Peptide Administration in Healthy Individuals

This study is a randomized, double-blind, placebo-controlled Phase 1 Clinical Trial of 24 healthy individuals to test the safety, tolerability and pharmacokinetics of a single subcutaneous administration of Serpin Peptide 16 (SP16), a Serine Protease Inhibitor (Serpin)-like, small peptide agonist of the Low Density Lipoprotein Receptor-like Protein 1 (LRPP1) hypothesized to have anti-inflammatory activity.

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Key information

Age range

18 year–59 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Virginia Commonwealth University

Richmond, Virginia, 23298, United States

About this study

One of the major determinants for outcome in patients with acute myocardial infarction (AMI) is the degree of inflammatory response. SP16 is a synthetic anti-inflammatory peptide developed to reproduce the anti-inflammatory activities of naturally occurring Serpins and has been tested as a treatment for AMI in mice. This Phase I trial will be the first to test the hypothesis that a single subcutaneous administration of SP16 is safe and well tolerated in healthy individuals, while also assessing the pharmacokinetic parameters of three different dosages. Participants will undergo direct clinical monitoring for up to 12 hours after drug administration. Additionally, participants will follow up with the same assessments at 24 hours, 48-72 hours and 7 days post drug administration.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Written informed consent
  • Age 18 to 59 years
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Ability to take oral medication and be willing to adhere to the medication regimen
  • For females of reproductive potential: Use of highly effective contraception
  • For males of reproductive potential: Use of condoms

Exclusion criteria

  • Acute or chronic illness affecting organ function or requiring medications (including, but not limited to, cardiovascular, hepatic, renal hematologic, neurologic, dermatologic, psychiatric, or rheumatologic disease);
  • Febrile illness within the previous 14 days;
  • Known allergic reactions to components of the study agent;
  • Treatment with another investigational drug or other intervention within 30 days;
  • Current tobacco use or tobacco use within 60 days;
  • Household contacts who are immunocompromised;
  • Chronic infection(s) (of any kind);
  • Malignancy (of any kind);
  • Substance abuse disorder(s);
  • Pregnancy or breastfeeding;
  • Any other conditions that would place the subject at increased risk of adverse events or interfere with the conduct or interpretation of the study, in the opinion of the investigators.

Treatment and study plan

SP16

Drug

subcutaneous injection of experimental anti-inflammatory drug

Placebos

Drug

subcutaneous injection of sterile saline

Primary outcomes

  1. Preliminary Safety Assessment: Occurence of adverse events

    Time frame: 7 days follow-up

    Occurence of adverse events

Secondary outcomes

  1. Volume of distribution of SP16 in healthy subjects

    Time frame: 7 days

    Population estimate of volume of distribution will be calculated using non-compartmental analysis

  2. Clearance of SP16 in healthy subjects

    Time frame: 7 days

    Population estimate of clearance will be calculated using non-compartmental analysis

Sponsors and collaborators

Lead sponsor

Serpin Pharma, LLC

Other

Collaborators

  • George Mason University
  • Virginia Commonwealth University

Registry information

Official study title

Safety, Tolerability and Pharmacokinetics of a Single Subcutaneous Administration of SP16-a SERPIN-like, Small Peptide Agonist of the Low Density Lipoprotein-like Receptor 1-in Healthy Individuals

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Aug 29, 2018
Registry last updated
Jul 28, 2021

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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