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Completed

NCT Number: NCT00583544

A Safety and Tolerability Single Ascending Dose Study in Healthy Volunteers

Targacept, Inc. is studying TC-2216 for a potential role in the treatment of central nervous system (CNS) neurobiological disorders in anticipation of seeking an indication in depression and/or anxiety.

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Key information

Conditions

Age range

18 year–40 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Forenap Pharma

Rouffache, France

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Male subjects aged 18-40 years old (both ages included).
  • Subjects must be in good health as determined by their medical history, physical examination, psychological examination, ECG, vital signs, standard EEG and laboratory tests. A volunteer with a clinical abnormality may be included only if the Investigator or his designee considers that the abnormality will not introduce additional risk factor for the subject's health, or interfere with the study objectives.
  • Subjects with a body mass index within the range 18-29 kg/m2 and a weight within the range of 60-90 kg.
  • Non-smoker subjects (a cotinine test will be performed at screening and Day -1
  • Subjects must be able to refrain from consuming xanthine containing beverages, and must refrain from intensive physical exercise during the study conduct (until the end of study visit).
  • Subjects must have signed an informed consent form indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study and comply with the study procedures and restrictions.
  • Subjects must be affiliated with, or a beneficiary of, a French social security system.

Exclusion criteria

Potential subjects who meet any of the following criteria will be excluded from participating in the study:

  • Any clinically relevant acute or chronic diseases which could interfere with the subjects safety during the trial, or expose them to undue risk, or which could interfere with the study objectives.
  • History or presence of gastrointestinal, hepatic, or renal disease or other condition known to interfere with the absorption, distribution, metabolism or excretion of drugs.
  • Any history of drug or other significant allergy.
  • Likely to need any treatment (including dental care) during the study period.
  • Donation of one or more units of blood within 90 days prior to the screening.
  • Use of any prescription or over-the-counter medication within 14 days prior to admission on Day-1 (not including paracetamol in the range of 1gr/day). In addition any medications with central effects are prohibited for a period equal to 5 x half-life prior to admission (Day-1), should this period be longer than 14 days.
  • Alcohol consumption > 40 g alcohol/day (1 glass (25 cl) of beer with 3° of alcohol = 7.5 g, or 1 glass (25 cl) of beer with 6° of alcohol = 15 g, or 1 glass (12.5 cl) of wine with 10° of alcohol = 12 g, or 1 glass (4cl) of aperitif with 42° of alcohol = 17 g).
  • Positive alcotest at screening and Day -1 .
  • Positive test result on hepatitis B surface antigen, hepatitis C antibody.
  • Positive test result on HIV 1 and 2 serology.
  • Excessive daily consumption of xanthines containing drinks (i.e > 500 mg/day of caffeine).

Treatment and study plan

TC-2216

Drug

Multiple ascending dose groups will be explored.

Primary outcomes

  1. hematology, biochemistry, urine analysis, vital sign, ECG, adverse events.

    Time frame: 4 days

Secondary outcomes

  1. plasma and urine pharmacokinetics, Pharmaco EEG, Bond-Lader Visual Analogue Scal

    Time frame: 4 days

Sponsors and collaborators

Lead sponsor

Targacept Inc.

Industry

Registry information

Official study title

A Double Blind, Sequential, Ascending Single Dose, Placebo-Controlled Safety, Tolerability, and Pharmacokinetic and Pharmacodynamic Study of TC-2216 in Healthy Young Male Volunteers.

Acronym: SRD

Important dates

Study start
2007
Primary completion
2008
Study completion
2008
First posted
Dec 31, 2007
Registry last updated
Jul 18, 2008

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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