SXC-2023 Cocaine Interaction Study
Cocaine Use Disorder
Bottom Line
View on ClinicalTrials.gov: NCT06343532 ↗Study Design & Population
- Study type
- Interventional
- Phase
- Phase 1
- Interventions
- SXC-2023 (Drug); SXC-2023 Placebo (Drug)
- Age
- Adult · 18+ yrs
- Sex
- All
- Sponsor
- National Institute on Drug Abuse (NIDA)
- Primary completion
- Dec 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Total Number of Treatment-Emergent Adverse Events (Safety and Tolerability) of Oral SXC-2023 Co-administered With Intravenous Cocaine |
99; 132 | — |
| PRIMARY Maximum Pulse (After 20 mg i.v. Cocaine) |
92.2; 100.6 | — |
| PRIMARY Maximum Pulse (After 40 mg i.v. Cocaine) |
105.8; 112.8 | — |
| PRIMARY Maximum Systolic Blood Pressure (After 20 mg i.v. Cocaine) |
130.7; 132.9 | — |
| PRIMARY Maximum Systolic Blood Pressure (After 40 mg i.v. Cocaine) |
138.3; 139.9 | — |
| PRIMARY Maximum Diastolic Blood Pressure (After 20 mg i.v. Cocaine) |
82.6; 83.6 | — |
| PRIMARY Maximum Diastolic Blood Pressure (After 40 mg i.v. Cocaine) |
85.7; 87.8 | — |
Summary
Eligibility Criteria
Inclusion Criteria: In order to participate in the study, participants must:
- Be participants who are cocaine-experienced and not seeking treatment for cocaine use disorder.
- Males and females between 18 and 59 years of age, inclusive.
- The masculine / feminine gender is used without any discrimination and with the aim to lighten the text.
- Have a body mass index (BMI) within a range of 17.0 to 36.0 kg/m2 and a minimum weight of at least 50.0 kg at screening.
- Have experience using cocaine by the smoked or i.v. route at least 6 times over the participant's lifetime prior to clinic intake (Day -3) and at least one use within the past 3 months.
- Provide a urine sample positive for cocaine at least once during screening (Days -28 to -4) and a urine test negative for cocaine at clinic intake.
- Be able to verbalize understanding of consent form, able to provide written informed consent, and verbalize willingness to complete study procedures.
- A female study participant must meet one of the following criteria:
- If of childbearing potential - agrees to use one of the accepted contraceptive regimens from at least 30 days prior to the first administration of the study medication, during the study, and for at least 30 days after the last dose of the study medication. An acceptable method of contraception includes one of the following:
i. Abstinence from heterosexual intercourse ii. Hormonal contraceptives (oral/injectable/implant/insertable hormonal birth control products, transdermal patch) iii. Intrauterine device (with or without hormones) OR agrees to use a double barrier method (e.g., condom and spermicide) during the study and for at least 30 days after the last dose of the study medication.
- If a female of non-childbearing potential - should be surgically sterile (i.e., has undergone complete hysterectomy, bilateral oophorectomy, or tubal ligation/occlusion) or in a menopausal state (at least 1 year without menses), as confirmed by FSH levels (≥ 40 mIU/mL).
A male study participant that engages in sexual activity that has the risk of pregnancy must agree to use a double barrier method (e.g., condom and spermicide) and agree to not donate sperm during the study and for at least 90 days after the last dose of the study medication.
- Be able to comply with protocol requirements, rules and regulations of the study site, and be likely to complete all the study treatments.
Exclusion Criteria: In order to participate in the study, participants must not:
- Have a current or past history of seizure disorder, including alcohol- or stimulant-related seizure, febrile seizure, or significant family history of idiopathic seizure disorder.
- Have any previous medically adverse reaction to cocaine, including loss of consciousness, chest pain, paranoid reaction or seizure.
- Have clinically significant findings in the opinion of an investigator based on the MINI (version 7.0) neuropsychiatric interview.
- Be pregnant or lactating.
- Have a sitting systolic blood pressure > 140 mmHg, diastolic blood pressure > 90 mmHg and heart rate > 100 beats per minute at screening and clinic intake.
- Have a history of liver disease or current elevation of aspartate aminotransferase (AST), alanine aminotransferase (ALT), 2 × the upper limit of normal.
- Blood donation (excluding plasma donation) of approximately 500 mL within 56 days prior to screening.
- Plasma donation within 7 days prior to screening.
- Treatment with an investigational drug within 30 days or 5 times the half-life (whichever is longer) prior to screening.
- Have any clinically significant finding on medical history, physical examination, clinical laboratory test, vital signs or ECGs that contraindicate participation in the study.
- Have a history of suicide attempts or current or recent evidence of suicidal ideation in the past 12 months based on the Columbia-Suicide Severity Rating Scale (C-SSRS).
- Have a positive urine drug screen upon clinic intak
Data sourced from ClinicalTrials.gov (NCT06343532). 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.