SXC-2023 Cocaine Interaction Study
Phase 1, Double-Blind, Placebo-Controlled, Parallel Group Study to Assess Potential Interactions Between Intravenous Cocaine and Oral SXC-2023
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 1
Contacts and Locations
Study Contact
Study Contact
- Name: Debra Kelsh, MD
- Phone Number: 913-696-1601
- Email: DKelsh@altasciences.com
Study Locations
-
-
Kansas
-
Overland Park, Kansas, United States, 66212
- Altasciences Clinical Kansas, Inc.
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
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 intake (Day -3) for any of the following drugs: alcohol, amphetamine/methamphetamine, barbiturates, benzodiazepines, buprenorphine, cocaine, fentanyl, 3,4-methylenedioxymethamphetamine (MDMA), methadone, phencyclidine/phenylcyclohexyl piperidine (PCP), propoxyphene, and opioids (e.g., codeine, heroin, morphine, oxycodone, etc.). If a participant presents with a positive urine drug screen for cocaine or alcohol at clinic intake (Day -3), the participant may be rescheduled one time at the discretion of an investigator or designee as long as clinic intake is within the total screening window.
- Have used any prescription drugs within 14 days of clinic intake or non-prescription drugs or herbal remedies within 7 days of clinic intake.
- Be unable to distinguish between a 20 mg and 40 mg dose of cocaine i.v. based on the high effects VAS at either the 5 or 10 minute time point during the screening infusion.
- Have a positive serology for Hepatitis B surface antigen (HBsAg), Hepatitis C antibody (HCVab), or human immunodeficiency virus (HIV).
- Have positive results for a coronavirus disease 2019 (COVID-19) test performed after screening is complete and participant is confirmed, but prior to admission.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: SXC-2023
SXC-2023: 800mg once a day for 7 days
|
200 mg capsules
|
|
Placebo Comparator: SXC-2023 Placebo
Placebo: 800mg once a day for 7 days
|
200 mg capsules
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Total Number of Treatment-Emergent Adverse Events (Safety and Tolerability) of Oral SXC-2023 Co-administered With Intravenous Cocaine
Time Frame: Study Days -2,1,2,8,9,11
|
Assessing the number of treatment emergent adverse events using the most recent version of the Medical Dictionary of Regulatory Activities (MedDRA) preferred terms. Adverse events were either reported by the participants or determined by clinically significant abnormal findings on: i. Physical examination ii. Measurement of vital signs (heart rate, blood pressure) iii. Clinical laboratory findings |
Study Days -2,1,2,8,9,11
|
|
Maximum Pulse (After 20 mg i.v. Cocaine)
Time Frame: Study Day 8, 30 min pre till 5 hours post cocaine infusion
|
Maximum heart rate (bpm) after cocaine infusion 20 mg i.v.
|
Study Day 8, 30 min pre till 5 hours post cocaine infusion
|
|
Maximum Pulse (After 40 mg i.v. Cocaine)
Time Frame: Study Day 9, 30 min pre till 5 hours post cocaine infusion
|
Maximum heart rate (bpm) after cocaine infusion 40 mg i.v.
|
Study Day 9, 30 min pre till 5 hours post cocaine infusion
|
|
Maximum Systolic Blood Pressure (After 20 mg i.v. Cocaine)
Time Frame: Study Day 8, 30 min pre till 5 hours post cocaine infusion
|
Maximum Systolic Blood Pressure (mmHg) after cocaine infusion 20 mg i.v.
|
Study Day 8, 30 min pre till 5 hours post cocaine infusion
|
|
Maximum Systolic Blood Pressure (After 40 mg i.v. Cocaine)
Time Frame: Study Day 9, 30 min pre till 5 hours post cocaine infusion
|
Maximum Systolic Blood Pressure (mmHg) after cocaine infusion 40 mg i.v.
|
Study Day 9, 30 min pre till 5 hours post cocaine infusion
|
|
Maximum Diastolic Blood Pressure (After 20 mg i.v. Cocaine)
Time Frame: Study Day 8, 30 min pre till 5 hours post cocaine infusion
|
Maximum Diastolic Blood Pressure (mmHg) after cocaine infusion 20 mg i.v.
|
Study Day 8, 30 min pre till 5 hours post cocaine infusion
|
|
Maximum Diastolic Blood Pressure (After 40 mg i.v. Cocaine)
Time Frame: Study Day 9, 30 min pre till 5 hours post cocaine infusion
|
Maximum Diastolic Blood Pressure (mmHg) after cocaine infusion 40 mg i.v.
|
Study Day 9, 30 min pre till 5 hours post cocaine infusion
|
Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Investigators
Investigators
- Principal Investigator: Debra Kelsh, MD, Altasciences Clinical Kansas, Inc.
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
Other Study ID Numbers
- NIDA-SXC-Ph1b-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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