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Cannabis Effects on Antiretroviral Therapy Pharmacokinetics and Neurotoxicity

Primary Purpose

HIV, Cannabis Use

Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
THC Cannabis
CBD Cannabis
Placebo
Sponsored by
University of California, San Diego
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for HIV

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria for All Visits:

  1. Age 18 or older;
  2. Capacity to provide informed consent;
  3. Presence of HIV infection by a standard diagnostic test;
  4. On a stable ART regimen for at least 3 months;
  5. Taking an ART drug that is metabolized by either cytochrome p450 (CYP) isozymes or by uridine 5'-diphospho-glucuronosyltransferase (UGT) isozymes; and
  6. Willing to abstain from cannabis for at least 24 hours prior to the Phase 1 assessment.
  7. Willing to abstain from grapefruit juice consumption for 4 weeks prior to the Phase 1 assessment.

Additional Inclusion Criteria for participation in Phase 2 (interventional):

  1. Treatment with an integrase inhibitor (i.e. dolutegravir);
  2. Use of cannabis in the past two years without a severe adverse reaction (e.g., disorientation, paranoia, or hallucinations). The two-year cutoff is to ensure exposure to modern cannabis, which is more likely to match the drug concentrations administered in this study;
  3. Willing to refrain from driving or operating heavy machinery after the visit; and
  4. Willing to abstain from cannabis for at least 48 hours prior to the cannabis administration visits.
  5. Willing to abstain from grapefruit juice consumption for 4 weeks prior to cannabis administration and during the administration visits

Exclusion Criteria for All Visits:

  1. Traumatic brain injury, including head injury with loss of consciousness for greater than 30 minutes or resulting in neurologic complications;
  2. Dementia, including Alzheimer's disease;
  3. History of stroke with residual neurologic sequelae;
  4. History of seizure disorder with a seizure in the past year;
  5. Severe psychiatric disorder (e.g., schizophrenia) that might make the person's participation in the study unsafe;
  6. Substance or alcohol use disorder in the past 12 months;
  7. Contraindications to lumbar puncture for those consenting to lumbar puncture (e.g., coagulopathy).

Additional Exclusion Criteria for participation in the cannabis administration visits:

  1. Younger than 21 years (due to safety of cannabis in children and adolescents);
  2. Respiratory condition that would be exacerbated by inhaling vaporized cannabis (e.g., asthma or chronic obstructive pulmonary disease) or limited lung capacity that would prevent the individual from performing the Foltin puff procedure;
  3. History of cardiovascular disease, including myocardial infarction;
  4. Uncontrolled hypertension with systolic blood pressure greater than 160 mm Hg or a diastolic blood pressure greater than 100 mm Hg prior to study product administration;
  5. Resting pulse greater than 100 beats per minute prior to study product administration;
  6. Pregnancy as determined by a human chorionic gonadotropin urine test, women who are lactating, or unwillingness to prevent pregnancy during the cannabis administration portion of the study (using birth control in women of child-bearing age). Acceptable methods of birth control are: oral contraceptive pills, diaphragm, condom, progestin implant, intrauterine contraceptive device, sterilization, etc;
  7. Active opportunistic infection or malignancy requiring treatment;
  8. Unintentional loss of 10% or more of body weight during the previous 6 months;
  9. CD4+ T-cell count less than 200 cells/µL;
  10. Estimated glomerular filtration rate < 40 mL/minute, indicative of renal dysfunction;
  11. Hepatic transaminases > 2 times the upper limit of normal;
  12. Current severe depressive symptoms (BDI-II score ≥ 31) or suicidal ideation;
  13. Known sensitivity to acetaminophen (the probe for UGT activity);
  14. Current use of substances that could have adverse interactions with acetaminophen or cannabis (e.g., grapefruit juice).

Sites / Locations

  • Ucsd Hnrp-CmcrRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

THC Cannabis

CBD Cannabis

Placebo

Arm Description

11.86% THC/ 1.12% CBD

0.35% THC/ 11.27% CBD

≤ 0.01% THC/ ≤ 0.01% CBD

Outcomes

Primary Outcome Measures

1a i. Antiretroviral therapy (ART) drug concentration in blood
This will be done separately for participants who use ART drugs that are predominantly metabolized by cytochrome P450 (CYP) or uridine 5'-diphospho-glucuronosyltransferase (UGT) (estimated N=60 in each).
1a ii. Cerebrospinal fluid (CSF)/plasma ratio of ART drug concentrations
This will be done separately for CYP and UGT groups (estimated N=60 in each).
1a iii. Change in ART drug concentrations in blood
This will be done separately for CYP and UGT groups (estimated N=60 in each).
1a iv. Change in CSF/plasma ratio of ART drug concentrations
This will be done separately for CYP and UGT groups (estimated N=60 in each).
1b i. Effects of placebo, THC, and CBD on ART drug concentration
The investigators will use a mixed effects model to assess effects of acute cannabis treatment (placebo, THC, or CBD: N=40) on the area under the time-drug concentration curve.
1b ii. Effects of placebo, THC and CBD on the CSF/plasma ratio of ART drug concentrations
The investigators will use a mixed effects model to assess effects of acute cannabis treatment (placebo, THC, or CBD: N=40) on CSF/plasma ratio of ART drug concentrations
1b iii. Comparison between the effects of placebo and THC on ART pharmacokinetics and between the effects of placebo and CBD on ART pharmacokinetics
Comparison of the the area under the time-concentration curve of ART pharmacokinetics for placebo and THC and placebo and CBD (n=40). The effect size will be measured as the standardized difference in mean outcomes between any two groups (Cohen's d).
1b iv. Comparison between the effects of placebo and CBD on the CSF/plasma ratio of ART drug concentrations and between the effects of placebo and THC on the CSF/plasma ratio of ART drug concentrations
Comparison of the the CSF/plasma ratio of ART drug concentrations with placebo and CBD and with placebo and THC (n=40). The effect size will be measured as the standardized difference in mean outcomes between any two groups (Cohen's d).
2a. Effects of chronic cannabis use on the CSF/serum albumin ratio and P-glycoprotein (P-gp) expression.
Multivariate linear regression will be used to regress markers of blood-brain barrier integrity and P-gp on cannabis use (n = 120), then ART drug concentrations on blood-brain barrier integrity and P-gp separately for the UGT and CYP groups
2b. Examine the correlation between ART concentration in CSF and blood during placebo treatment compared to THC and CBD administration.
The investigators will use a mixed effects model to evaluate the effects of cannabis on the correlation between ART concentration in CSF and blood (n = 40).
2c. Effects of THC or CBD on uridine 5'-diphospho-glucuronosyltransferase (UGT) activity compared to placebo.
The investigators will use a mixed effects model to examine the effects of drug treatment on UGT metabolism (n = 40).
3a. i. Correlation between CD4+ T-cell count and ART drug concentration.
Multivariable linear regressions will be used for testing correlation between CD4+ T-cell count and ART drug concentration (N=60 in each UGT and CYP groups).
3a. ii. Correlation between HIV DNA and ART drug concentration.
Multivariable logistic regressions will be used for testing correlation between HIV DNA and ART drug concentration (N=60 in each UGT and CYP groups).
3b i. Effects of cannabis use on the correlation between ART and neurocognitive performance.
The total cognitive outcome from the National Institutes of Health Toolbox will be regressed in multivariable models on ART drug concentration and cannabis use, their interaction, and known confounders and relevant covariates. Values range from 0 to 100 with lower values being worse.
3b ii. Effects of cannabis use on the correlation between ART and depression.
Depression (measured with the Beck Depression Inventory-II) will be regressed in multivariable models on ART drug concentration and cannabis use, their interaction, and known confounders and relevant covariates.
3b iii. Effects of cannabis use on the correlation between ART and emotional health.
The National Institutes of Health Toolbox-Emotional Battery outcome, Negative Affect, will be regressed in multivariable models on ART drug concentration and cannabis use, their interaction, and known confounders and relevant covariates. This measure ranges between 0 and 100 with higher values reflecting more Negative Affect.
3b iv. Effects of cannabis use on the correlation between ART and emotional health.
The National Institutes of Health Toolbox-Emotional Battery outcome, Social Satisfaction, will be regressed in multivariable models on ART drug concentration and cannabis use, their interaction, and known confounders and relevant covariates. This measure ranges between 0 and 100 with lower values reflecting worse Social Satisfaction.
3b v. Effects of cannabis use on the correlation between ART and emotional health.
The National Institutes of Health Toolbox-Emotional Battery outcome, Psychological Wellbeing, will be regressed in multivariable models on ART drug concentration and cannabis use, their interaction, and known confounders and relevant covariates. This measure ranges between 0 and 100 with lower values reflecting worse Psychological Wellbeing.
3b vi. Effects of cannabis use on the correlation between ART and neurotoxicity.
A measure of neurotoxicity (mitochondrial DNA) will be regressed in multivariable models on ART drug concentration and cannabis use, their interaction, and known confounders and relevant covariates.
3b vii. Effects of cannabis use on the correlation between ART and neurotoxicity.
A measure of neurotoxicity (8-hydroxydeoxyguanosine) will be regressed in multivariable models on ART drug concentration and cannabis use, their interaction, and known confounders and relevant covariates.
3b viii. Effects of cannabis use on the correlation between ART and neurotoxicity.
A measure of neurotoxicity (F2-isoprostane) will be regressed in multivariable models on ART drug concentration and cannabis use, their interaction, and known confounders and relevant covariates.

Secondary Outcome Measures

1b v. Comparison between the effects of THC and CBD on ART pharmacokinetics.
Comparison of the treatment arm to the the area under the time-concentration curve of ART pharmacokinetics (n=40).
1b vi. Comparison between the effects of THC and CBD on the CSF/plasma ratio of ART drug concentrations.
Comparison of treatment arm to the CSF/plasma ratio of ART drug concentrations.

Full Information

First Posted
February 19, 2021
Last Updated
October 2, 2023
Sponsor
University of California, San Diego
Collaborators
Center for Medicinal Cannabis Research
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1. Study Identification

Unique Protocol Identification Number
NCT04800159
Brief Title
Cannabis Effects on Antiretroviral Therapy Pharmacokinetics and Neurotoxicity
Official Title
Cannabis Effects on Antiretroviral Therapy Pharmacokinetics and Neurotoxicity
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 19, 2021 (Actual)
Primary Completion Date
January 30, 2025 (Anticipated)
Study Completion Date
April 30, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, San Diego
Collaborators
Center for Medicinal Cannabis Research

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will address whether cannabis affects antiretroviral therapy (ART) drug concentrations, mood, and thinking. The project will have two phases. Phase 1 is an observational study, in which 120 people will be assessed to evaluate the effects of chronic cannabis use on ART drug concentrations, mood, and thinking. In Phase 2, the study will administer cannabis (or placebo) to 40 people to examine its acute effects on ART drug concentrations.
Detailed Description
People with human immunodeficiency virus (HIV) commonly use cannabis but whether cannabis affects the antiretroviral therapy (ART) that treats HIV is not well known. Cannabis can inhibit the activity of enzymes that metabolize and eliminate ART drugs from the body, which could result in higher concentrations of ART drugs in the body. Cannabis may also affect the distribution of ART drugs into the brain, which could have both beneficial (e.g., better HIV control) and detrimental (e.g., toxicity) effects. The effects of cannabis may are likely influenced by factors like how much is used (e.g., light vs. heavy use) and the route of use (e.g., smoked vs. ingested). This study will address whether cannabis affects ART concentrations in blood and cerebrospinal fluid as well as mood, and thinking. The project will have two phases. Phase 1 is an observational study, in which 120 people will be assessed once to evaluate the effects of chronic cannabis use on ART drug concentrations, mood, and thinking. In Phase 2, the study will administer cannabis (or placebo) to 40 people to examine its acute effects on ART drug concentrations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV, Cannabis Use

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Model Description
The interventional component of the project (Phase 2) will have a randomized cross-over design that randomly assigns the order of the administration of the three study products (placebo, cannabis with higher concentration of tetrahydrocannabinol (THC) and lower concentration of cannabidiol (CBD), or cannabis with higher CBD concentration and lower THC concentration). The cannabis administration phase of this study will compare the study products to: 1) ART concentrations in blood and CSF and 2) measures of uridine 5'-diphospho-glucuronosyltransferase (UGT) activity.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Participants will randomly receive one of the study products at each visit. All participants will receive all three of the study products. Allocation assignment of visits will be assigned using a randomization string provided by the statistician. The allocation schedule will be kept in the pharmacy and concealed from all other study personnel.
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
THC Cannabis
Arm Type
Active Comparator
Arm Description
11.86% THC/ 1.12% CBD
Arm Title
CBD Cannabis
Arm Type
Active Comparator
Arm Description
0.35% THC/ 11.27% CBD
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
≤ 0.01% THC/ ≤ 0.01% CBD
Intervention Type
Drug
Intervention Name(s)
THC Cannabis
Other Intervention Name(s)
Marijuana
Intervention Description
Vaporization of cannabis
Intervention Type
Drug
Intervention Name(s)
CBD Cannabis
Other Intervention Name(s)
Marijuana
Intervention Description
Vaporization of cannabis
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Marijuana with < 0.01% of THC and CBD
Intervention Description
Vaporization of placebo
Primary Outcome Measure Information:
Title
1a i. Antiretroviral therapy (ART) drug concentration in blood
Description
This will be done separately for participants who use ART drugs that are predominantly metabolized by cytochrome P450 (CYP) or uridine 5'-diphospho-glucuronosyltransferase (UGT) (estimated N=60 in each).
Time Frame
Cross-sectional; measured before ART ingestion
Title
1a ii. Cerebrospinal fluid (CSF)/plasma ratio of ART drug concentrations
Description
This will be done separately for CYP and UGT groups (estimated N=60 in each).
Time Frame
Cross-sectional; measured before ART ingestion
Title
1a iii. Change in ART drug concentrations in blood
Description
This will be done separately for CYP and UGT groups (estimated N=60 in each).
Time Frame
2 hours; measured before ART ingestion and at 2 hours after the ART ingestion
Title
1a iv. Change in CSF/plasma ratio of ART drug concentrations
Description
This will be done separately for CYP and UGT groups (estimated N=60 in each).
Time Frame
2 hours; measured before ART ingestion and at 2 hours after the ART ingestion
Title
1b i. Effects of placebo, THC, and CBD on ART drug concentration
Description
The investigators will use a mixed effects model to assess effects of acute cannabis treatment (placebo, THC, or CBD: N=40) on the area under the time-drug concentration curve.
Time Frame
5 hours
Title
1b ii. Effects of placebo, THC and CBD on the CSF/plasma ratio of ART drug concentrations
Description
The investigators will use a mixed effects model to assess effects of acute cannabis treatment (placebo, THC, or CBD: N=40) on CSF/plasma ratio of ART drug concentrations
Time Frame
5 hours
Title
1b iii. Comparison between the effects of placebo and THC on ART pharmacokinetics and between the effects of placebo and CBD on ART pharmacokinetics
Description
Comparison of the the area under the time-concentration curve of ART pharmacokinetics for placebo and THC and placebo and CBD (n=40). The effect size will be measured as the standardized difference in mean outcomes between any two groups (Cohen's d).
Time Frame
3 to 11 days
Title
1b iv. Comparison between the effects of placebo and CBD on the CSF/plasma ratio of ART drug concentrations and between the effects of placebo and THC on the CSF/plasma ratio of ART drug concentrations
Description
Comparison of the the CSF/plasma ratio of ART drug concentrations with placebo and CBD and with placebo and THC (n=40). The effect size will be measured as the standardized difference in mean outcomes between any two groups (Cohen's d).
Time Frame
3 to 11 days
Title
2a. Effects of chronic cannabis use on the CSF/serum albumin ratio and P-glycoprotein (P-gp) expression.
Description
Multivariate linear regression will be used to regress markers of blood-brain barrier integrity and P-gp on cannabis use (n = 120), then ART drug concentrations on blood-brain barrier integrity and P-gp separately for the UGT and CYP groups
Time Frame
3 to 11 days
Title
2b. Examine the correlation between ART concentration in CSF and blood during placebo treatment compared to THC and CBD administration.
Description
The investigators will use a mixed effects model to evaluate the effects of cannabis on the correlation between ART concentration in CSF and blood (n = 40).
Time Frame
3 to 11 days
Title
2c. Effects of THC or CBD on uridine 5'-diphospho-glucuronosyltransferase (UGT) activity compared to placebo.
Description
The investigators will use a mixed effects model to examine the effects of drug treatment on UGT metabolism (n = 40).
Time Frame
3 to 11 days
Title
3a. i. Correlation between CD4+ T-cell count and ART drug concentration.
Description
Multivariable linear regressions will be used for testing correlation between CD4+ T-cell count and ART drug concentration (N=60 in each UGT and CYP groups).
Time Frame
Up to 5 weeks: baseline to administration visits
Title
3a. ii. Correlation between HIV DNA and ART drug concentration.
Description
Multivariable logistic regressions will be used for testing correlation between HIV DNA and ART drug concentration (N=60 in each UGT and CYP groups).
Time Frame
Up to 5 weeks: baseline to administration visits
Title
3b i. Effects of cannabis use on the correlation between ART and neurocognitive performance.
Description
The total cognitive outcome from the National Institutes of Health Toolbox will be regressed in multivariable models on ART drug concentration and cannabis use, their interaction, and known confounders and relevant covariates. Values range from 0 to 100 with lower values being worse.
Time Frame
3 to 11 days
Title
3b ii. Effects of cannabis use on the correlation between ART and depression.
Description
Depression (measured with the Beck Depression Inventory-II) will be regressed in multivariable models on ART drug concentration and cannabis use, their interaction, and known confounders and relevant covariates.
Time Frame
3 to 11 days
Title
3b iii. Effects of cannabis use on the correlation between ART and emotional health.
Description
The National Institutes of Health Toolbox-Emotional Battery outcome, Negative Affect, will be regressed in multivariable models on ART drug concentration and cannabis use, their interaction, and known confounders and relevant covariates. This measure ranges between 0 and 100 with higher values reflecting more Negative Affect.
Time Frame
3 to 11 days
Title
3b iv. Effects of cannabis use on the correlation between ART and emotional health.
Description
The National Institutes of Health Toolbox-Emotional Battery outcome, Social Satisfaction, will be regressed in multivariable models on ART drug concentration and cannabis use, their interaction, and known confounders and relevant covariates. This measure ranges between 0 and 100 with lower values reflecting worse Social Satisfaction.
Time Frame
3 to 11 days
Title
3b v. Effects of cannabis use on the correlation between ART and emotional health.
Description
The National Institutes of Health Toolbox-Emotional Battery outcome, Psychological Wellbeing, will be regressed in multivariable models on ART drug concentration and cannabis use, their interaction, and known confounders and relevant covariates. This measure ranges between 0 and 100 with lower values reflecting worse Psychological Wellbeing.
Time Frame
3 to 11 days
Title
3b vi. Effects of cannabis use on the correlation between ART and neurotoxicity.
Description
A measure of neurotoxicity (mitochondrial DNA) will be regressed in multivariable models on ART drug concentration and cannabis use, their interaction, and known confounders and relevant covariates.
Time Frame
3 to 11 days
Title
3b vii. Effects of cannabis use on the correlation between ART and neurotoxicity.
Description
A measure of neurotoxicity (8-hydroxydeoxyguanosine) will be regressed in multivariable models on ART drug concentration and cannabis use, their interaction, and known confounders and relevant covariates.
Time Frame
3 to 11 days
Title
3b viii. Effects of cannabis use on the correlation between ART and neurotoxicity.
Description
A measure of neurotoxicity (F2-isoprostane) will be regressed in multivariable models on ART drug concentration and cannabis use, their interaction, and known confounders and relevant covariates.
Time Frame
3 to 11 days
Secondary Outcome Measure Information:
Title
1b v. Comparison between the effects of THC and CBD on ART pharmacokinetics.
Description
Comparison of the treatment arm to the the area under the time-concentration curve of ART pharmacokinetics (n=40).
Time Frame
3 to 11 days
Title
1b vi. Comparison between the effects of THC and CBD on the CSF/plasma ratio of ART drug concentrations.
Description
Comparison of treatment arm to the CSF/plasma ratio of ART drug concentrations.
Time Frame
3 to 11 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria for All Visits: Age 18 or older; Capacity to provide informed consent; Presence of HIV infection by a standard diagnostic test; On a stable ART regimen for at least 1 month and with a suppressed viral load by self-report; Willing to abstain from cannabis for at least 24 hours prior to the Phase 1 assessment. Willing to abstain from grapefruit juice consumption for 4 weeks prior to the Phase 1 assessment. Additional Inclusion Criteria for participation in Phase 2 (interventional): Treatment with an integrase inhibitor (i.e. dolutegravir); Use of cannabis in the past two years without a severe adverse reaction (e.g., disorientation, paranoia, or hallucinations). The two-year cutoff is to ensure exposure to modern cannabis, which is more likely to match the drug concentrations administered in this study; Willing to refrain from driving or operating heavy machinery after the visit; and Willing to abstain from cannabis for at least 48 hours prior to the cannabis administration visits. Willing to abstain from grapefruit juice consumption for 4 weeks prior to cannabis administration and during the administration visits Exclusion Criteria for All Visits: Traumatic brain injury, including head injury with loss of consciousness for greater than 30 minutes or resulting in neurologic complications; Dementia, including Alzheimer's disease; History of stroke with residual neurologic sequelae; History of seizure disorder with a seizure in the past year; Severe psychiatric disorder (e.g., schizophrenia) that might make the person's participation in the study unsafe; Substance or alcohol use disorder in the past 3 months; Contraindications to lumbar puncture for those consenting to lumbar puncture (e.g., coagulopathy). Additional Exclusion Criteria for participation in the cannabis administration visits: Younger than 21 years (due to safety of cannabis in children and adolescents); Respiratory condition that would be exacerbated by inhaling vaporized cannabis (e.g., asthma or chronic obstructive pulmonary disease) or limited lung capacity that would prevent the individual from performing the Foltin puff procedure; History of cardiovascular disease, including myocardial infarction; Uncontrolled hypertension with systolic blood pressure greater than 160 mm Hg or a diastolic blood pressure greater than 100 mm Hg prior to study product administration; Resting pulse greater than 100 beats per minute prior to study product administration; Pregnancy as determined by a human chorionic gonadotropin urine test, women who are lactating, or unwillingness to prevent pregnancy during the cannabis administration portion of the study (using birth control in women of child-bearing age). Acceptable methods of birth control are: oral contraceptive pills, diaphragm, condom, progestin implant, intrauterine contraceptive device, sterilization, etc; Active opportunistic infection or malignancy requiring treatment; Unintentional loss of 10% or more of body weight during the previous 6 months; CD4+ T-cell count less than 200 cells/µL; Estimated glomerular filtration rate < 30 mL/minute, indicative of renal dysfunction; Hepatic transaminases > 2 times the upper limit of normal; Current severe depressive symptoms (BDI-II score ≥ 31) or suicidal ideation; Known sensitivity to acetaminophen (the probe for UGT activity); Current use of substances that could have adverse interactions with acetaminophen or cannabis (e.g., grapefruit juice).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Roberto Gallardo
Phone
619-543-5000
Email
hnrprecruitment@ucsd.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Scott Letendre, MD
Organizational Affiliation
UCSD
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ucsd Hnrp-Cmcr
City
San Diego
State/Province
California
ZIP/Postal Code
92103
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Roberto Gallardo
Phone
619-543-5000
Email
hnrprecruitment@ucsd.edu

12. IPD Sharing Statement

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Cannabis Effects on Antiretroviral Therapy Pharmacokinetics and Neurotoxicity

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