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Phase 1 Randomized, Double-Blind, Placebo-Controlled Study to Determine the Safety, Tolerability, and Pharmacokinetics of a Single Escalating Dose and Repeated Doses of CN-105 in Healthy Adult Subjects.

Publication ,  Journal Article
Guptill, JT; Raja, SM; Boakye-Agyeman, F; Noveck, R; Ramey, S; Tu, TM; Laskowitz, DT
Published in: J Clin Pharmacol
June 2017

Spontaneous intracranial hemorrhage (ICH) remains a devastating stroke subtype, affecting as many as 80,000 people annually in the United States and associated with extremely high mortality. In the absence of any pharmacological interventions demonstrated to improve outcome, care for patients with ICH remains largely supportive. Thus, despite advances in the understanding of ICH and brain injury, there remains an unmet need for interventions that improve neurologic recovery and outcomes. Recent research suggesting inflammation and APOE genotype play a role in modifying neurologic outcome after brain injury has led to the development of an APOE-derived peptide agent (CN-105). Preclinical studies have demonstrated that CN-105 effectively downregulates the inflammatory response in acute brain injury, including ICH. Following Investigational New Drug (IND) enabling studies in murine models, this first-in-human single escalating dose and multiple dose placebo-controlled clinical trial was performed to define the safety and pharmacokinetics (PK) of CN-105. A total of 48 subjects (12 control, 36 active) were randomized in this study; all subjects completed the study. No significant safety issues were identified with both dosing regimens, and PK analysis revealed linearity without significant drug accumulation. The median half-life in the terminal elimination phase of CN-105 following a single or repeated dosing regimen did not change (approximately 3.6 hours). With the PK and preliminary safety of CN-105 established, the drug is now poised to begin first-in-disease phase 2 clinical trials in patients with ICH who urgently need new therapeutic options.

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Published In

J Clin Pharmacol

DOI

EISSN

1552-4604

Publication Date

June 2017

Volume

57

Issue

6

Start / End Page

770 / 776

Location

England

Related Subject Headings

  • Pharmacology & Pharmacy
  • Neuroprotective Agents
  • Male
  • Humans
  • Healthy Volunteers
  • Female
  • Double-Blind Method
  • Anti-Inflammatory Agents
  • Adult
  • 3214 Pharmacology and pharmaceutical sciences
 

Citation

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Guptill, J. T., Raja, S. M., Boakye-Agyeman, F., Noveck, R., Ramey, S., Tu, T. M., & Laskowitz, D. T. (2017). Phase 1 Randomized, Double-Blind, Placebo-Controlled Study to Determine the Safety, Tolerability, and Pharmacokinetics of a Single Escalating Dose and Repeated Doses of CN-105 in Healthy Adult Subjects. J Clin Pharmacol, 57(6), 770–776. https://doi.org/10.1002/jcph.853
Guptill, Jeffrey T., Shruti M. Raja, Felix Boakye-Agyeman, Robert Noveck, Sarah Ramey, Tian Ming Tu, and Daniel T. Laskowitz. “Phase 1 Randomized, Double-Blind, Placebo-Controlled Study to Determine the Safety, Tolerability, and Pharmacokinetics of a Single Escalating Dose and Repeated Doses of CN-105 in Healthy Adult Subjects.J Clin Pharmacol 57, no. 6 (June 2017): 770–76. https://doi.org/10.1002/jcph.853.

Published In

J Clin Pharmacol

DOI

EISSN

1552-4604

Publication Date

June 2017

Volume

57

Issue

6

Start / End Page

770 / 776

Location

England

Related Subject Headings

  • Pharmacology & Pharmacy
  • Neuroprotective Agents
  • Male
  • Humans
  • Healthy Volunteers
  • Female
  • Double-Blind Method
  • Anti-Inflammatory Agents
  • Adult
  • 3214 Pharmacology and pharmaceutical sciences