Cannabidiol

A non-psychoactive phytocannabinoid.

Phase of research

Potential treatment - pre-clinical evidence

How it helps

Antiviral

Drug status

Used to treat other disease

2
Supporting references
0
Contradictory references
20
AI-suggested references
8
Clinical trials

General information

Cannabidiol is a phytocannabinoid without psychoactive activity. It has been shown to possess analgesic, anti-inflammatory, antineoplastic, and chemopreventive properties (NCIt).

Cannabidiol on DrugBank
Cannabidiol on PubChem
Cannabidiol on Wikipedia



Synonyms

CBD


Marketed as

EPIDIOLEX

 

Structure image - Cannabidiol

CCCCCC1=CC(=C(C(=C1)O)[C@@H]2C=C(CC[C@H]2C(=C)C)C)O


Supporting references

Link Tested on Impact factor Notes Publication date
Assessment of antiviral potencies of cannabinoids against SARS-CoV-2 using computational and in vitro approaches
3CLpro Small molecule In vitro In silico
in silico; Vero cells 5.16

Inhibited SARS-CoV-2 in vitro (IC50u202f=u202f7.91u202fμM in Vero cells).

Dec/05/2020
Cannabis compounds exhibit anti-inflammatory activity in vitro in COVID-19-related inflammation in lung epithelial cells and pro-inflammatory activity in macrophages
Small molecule In vitro
A549 cells; KG1 cells 4.00

The compound reduced IL-8 levels in A549 cells when used in concentration of 3 μg/mL. Lower or higher concentrations did not result in IL-8 levels' decrease, however (bell-shaped dose-response). Combination of CBD with other bioactive constituents of Cannabis extracts might lead to increase of pro-inflammatory cytokine production in macrophages.

Jan/14/2021

AI-suggested references

Link Publication date
Activity of THC, CBD, and CBN on Human ACE2 and SARS-CoV1/2 Main Protease to Understand Antiviral Defense Mechanism.
Oct/12/2021
Cannabidiol for COVID-19 Patients with Mild to Moderate Symptoms (CANDIDATE Study): A Randomized, Double-Blind, Placebo-Controlled Clinical Trial.
Oct/07/2021
Cannabidiol Inhibits In Vitro Human Liver Microsomal Metabolism of Remdesivir: A Promising Adjuvant for COVID-19 Treatment.
Jun/16/2020
In silico inquest reveals the efficacy of Cannabis in the treatment of post-Covid-19 related neurodegeneration.
Apr/02/2021
Could Cannabidiol Be a Treatment for Coronavirus Disease-19-Related Anxiety Disorders?
Feb/12/2021
Efficacy and Safety of Cannabidiol Plus Standard Care vs Standard Care Alone for the Treatment of Emotional Exhaustion and Burnout Among Frontline Health Care Workers During the COVID-19 Pandemic
Aug/02/2021
In search of preventive strategies: novel high-CBD Cannabis sativa extracts modulate ACE2 expression in COVID-19 gateway tissues
Nov/22/2020
Cannabidiol Modulates Cytokine Storm in Acute Respiratory Distress Syndrome Induced by Simulated Viral Infection Using Synthetic RNA.
Sep/02/2020
Cannabinoids Alleviate the LPS-Induced Cytokine Storm via Attenuating NLRP3 Inflammasome Signaling and TYK2-Mediated STAT3 Signaling Pathways In Vitro
Aug/09/2021
Targeting of Protein's Messenger RNA for Viral Replication, Assembly and Release in SARS-CoV-2 Using Whole Genomic Data From South Africa: Therapeutic Potentials of Cannabis Sativa L
Apr/25/2022
Pharmacological Modulators of Autophagy as a Potential Strategy for the Treatment of COVID-19.
Apr/15/2021
In Vitro Evaluation of the Activity of Terpenes and Cannabidiol against Human Coronavirus E229
Dec/13/2021
Reducing SARS-CoV-2 pathological protein activity with small molecules.
Apr/05/2021
Effect of cannabidiol on apoptosis and cellular interferon and interferon-stimulated gene responses to the SARS-CoV-2 genes ORF8, ORF10 and M protein
Jun/30/2022
Cannabidiol and Terpene Formulation Reducing SARS-CoV-2 Infectivity Tackling a Therapeutic Strategy
Jul/15/2021
The potential of cannabidiol in the COVID-19 pandemic: a hypothesis letter
Jul/16/2020
Cannabidiol (CBD) modulation of apelin in acute respiratory distress syndrome
Apr/26/2021
Intranasal temperature-sensitive hydrogels of cannabidiol inclusion complex for the treatment of post-traumatic stress disorder
Jan/24/2021
Cannabidiol inhibits SARS-Cov-2 spike (S) protein-induced cytotoxicity and inflammation through a PPARgamma-dependent TLR4/NLRP3/Caspase-1 signaling suppression in Caco-2 cell line
Feb/05/2022
New AKT-dependent mechanisms of anti-COVID-19 action of high-CBD Cannabis sativa extracts
Jun/06/2020

Clinical trials

ID Title Status Phase Start date Completion date
NCT04603781 CBD Oil for Reducing Emotional Impact of COVID-19 Recruiting Phase 2|Phase 3 Dec/04/2020 Dec/31/2021
  • Alternative id - 2020-07-0138
  • Interventions - Dietary Supplement: CBD Isolate|Dietary Supplement: Full Spectrum CBD Oil|Dietary Supplement: Broad-Spectrum CBD Oil|Dietary Supplement: Placebo Oil
  • Study type - Interventional
  • Study results - No Results Available
  • Locations - University of Texas at Austin, Laboratory for the Study of Anxiety Disorders, Austin, Texas, United States
  • Study designs - Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|Primary Purpose: Treatment
  • Enrollment - 160
  • Age - 18 Years to 75 Years   (Adult, Older Adult)
  • Outcome measures - PROMIS Emotional Distress Index|PROMIS Depression Scale|PROMIS Anxiety Scale|PROMIS Anger Scale|PROMIS Alcohol Negative Consequences Scale|PROMIS Sleep Disturbance Scale|COVID-19 Coping Self-Efficacy
NCT04504877 Burnout and Distress preventiOn With caNnabidiol in Front-line Health Care workerS deAling wIth COVID-19 Completed Phase 2|Phase 3 Jun/16/2020 Dec/16/2020
  • Alternative id - BONSAI Study
  • Interventions - Drug: Cannabidiol
  • Study type - Interventional
  • Study results - No Results Available
  • Locations - Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto - USP, Ribeirão Preto, SP, Brazil
  • Study designs - Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Triple (Care Provider, Investigator, Outcomes Assessor)|Primary Purpose: Prevention
  • Enrollment - 120
  • Age - 24 Years to 60 Years   (Adult)
  • Outcome measures - aMBI-HSS: Abbreviated Maslach Burnout Inventory - Human Services Survey|Brief measure for assessing generalized anxiety disorder: The GAD-7|PHQ-9: Patient´s Health Questionnaire-9|Change in proinflammatory cytokine concentration|Number of participants with treatment-related adverse events as assessed by CTCAE v5.0|Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5)
NCT04615949 Cannabidiol in Patients With COVID-19 and Cardiovascular Disease or Risk Factors Recruiting Phase 2|Phase 3 Apr/30/2021 Apr/01/2022
  • Alternative id - CARDIOL 100-03
  • Interventions - Drug: Cannabidiol, pharmaceutically produced with < 5 ppm THC|Drug: Placebo
  • Study type - Interventional
  • Study results - No Results Available
  • Locations - Valleywise Health Medical Center, Phoenix, Arizona, United States|Westchester General Hospital, Miami, Florida, United States|University of South Florida, Tampa, Florida, United States|Prairie Education and Research Cooperative, Springfield, Illinois, United States|Lutheran Health Physicians, Fort Wayne, Indiana, United States|Lowcountry Infectious Disease, Charleston, South Carolina, United States|PRX Research/Dallas Regional Medical Center, Mesquite, Texas, United States|University of Texas Health Science Center, San Antonio, Texas, United States|Baylor Scott & White Health - Temple, Temple, Texas, United States|Liga de Hipertensão arterial, Goiânia, Goiás, Brazil|Sociedade Hospitalar Angelina Caron, Campina Grande Do Sul, Parana, Brazil|Science Valley Research Institute, Campo Largo, Parana, Brazil|Universidade Estadual de Maringa, Maringa, Parana, Brazil|Hospital de Clinicas de Porto Alegre, Porto Alegre, Rio Grande Do Sul, Brazil|Instituto de Cardiologia do Rio Grande do Sul, Porto Alegre, Rio Grande Do Sul, Brazil|Hospital São Lucas PUCRS, Porto Alegre, Rio Grande Do Sul, Brazil|Irmandade Santa Casa de Misericórdia, Porto Alegre, Rio Grande Do Sul, Brazil|Núcleo de Ensino e Pesquisa do Instituto Mário Penna, Conjunto ACM, Santa Maria, Brazil|Fundação Pio XII - Hospital de Amor Barretos, Barretos, Sao Paulo, Brazil|Science Valley Research Institute- Hospital Municipal de Barueri Dr. Francisco Moran, Barueri, Sao Paulo, Brazil|IPECC-Instituto de Pesquisa Clínica de Campinas, Campinas, Sao Paulo, Brazil|Instituto do Coração do HCFMUSP, Cerqueira César, Sao Paulo, Brazil|SVRI- Irmandade de Santa Casa de Misercordia de Santos, Jabaquara, Sao Paulo, Brazil|Science Valley Research Institute, Morumbi, Sao Paulo, Brazil|Science Valley Research Institute, Santo André, Sao Paulo, Brazil|Fundação Faculdade Regional de Medicine de Sao Jose do Rio Preto (SJRP), São José Do Rio Preto, Sao Paulo, Brazil|IAMSPE - Instituto de Assitencia Medica do Servidor Público Estadual, São Paulo, Sao Paulo, Brazil|Hospital 9 de Julho, São Paulo, Sao Paulo, Brazil|Hucff- Ufrj, Rio De Janeiro, Brazil|Complexo Hospitalar de Niteroi- Centro de Pesquisa Clinica, Rio de Janeiro, Brazil|Charite Universitatsmedizin Berlin, Berlin, Germany|Medical School of Bradenburg Theodor Fontane (MHB), Neuruppin, Germany|TecSalud, Monterrey, Nuevo Leon, Mexico|Unidad Medica para la Salud Integral UMSI, San Nicolás De Los Garza, Nuevo Leon, Mexico|Centro para el Desarrollo de la Medicina Y de la Asistencia Medica Especializada, Culiacan, Sinaloa, Mexico
  • Study designs - Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|Primary Purpose: Prevention
  • Enrollment - 422
  • Age - 18 Years and older   (Adult, Older Adult)
  • Outcome measures - All-cause mortality|Requirement for ICU admission and/or ventilatory support|CV complications
NCT04731116 Cannabidiol Treatment for Severe and Critical Coronavirus (COVID-19) Pulmonary Infection Recruiting Phase 1|Phase 2 Jan/10/2021 Apr/30/2022
  • Alternative id - 0245-20-RMC
  • Interventions - Drug: Cannabidiol
  • Study type - Interventional
  • Study results - No Results Available
  • Locations - Rabin Medical Center, Petach Tikva, Israel
  • Study designs - Allocation: N/A|Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment
  • Enrollment - 40
  • Age - 18 Years and older   (Adult, Older Adult)
  • Outcome measures - Serum C-reactive protein (CRP) level|Serum ferritin level|Serum Interferon gamma-induced protein 10 (IP10) level|Serum IL-6 level|Serum TNF-related apoptosis-inducing ligand (TRAIL)|Study drug related adverse events|Patient adherence to the study protocol|Ratio of arterial oxygen partial pressure (PaO2) to fractional inspired oxygen (FiO2) ratio (PaO2/FiO2 ratio) for ventilated patients|Length of ventilation for ventilated patients|Length of stay in the ICU|Survival by day 28|Remission of respiratory symptoms|Documented infections up to discharge|Sequential organ failure assistance (SOFA) score
NCT04777981 (CBDRA60) to Prevent or Reduce Symptoms of COVID-19 and Prevention of Post-Acute Sequelae of SARS-CoV-2 Infection PASC Not yet recruiting Not Applicable Jul/01/2022 Dec/28/2022
  • Alternative id - 1001
  • Interventions - Dietary Supplement: CBDRA60 supplement|Dietary Supplement: Placebo
  • Study type - Interventional
  • Study results - No Results Available
  • Locations - Anewsha Therapeutics / Comco R&D, Hanover, Michigan, United States
  • Study designs - Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Double (Participant, Investigator)|Primary Purpose: Treatment
  • Enrollment - 60
  • Age - 18 Years and older   (Adult, Older Adult)
  • Outcome measures - Decreased hospitalization|Resolution of COVID-19 symptoms
NCT04467918 CANnabiDiol for CoviD-19 pATiEnts With Mild to Moderate Symptoms Active, not recruiting Phase 2|Phase 3 Jul/06/2020 Nov/16/2021
  • Alternative id - CANDIDATE study
  • Interventions - Drug: Cannabidiol|Other: PLACEBO
  • Study type - Interventional
  • Study results - No Results Available
  • Locations - Serviço de Assistência Médica e Social do Pessoal do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo, Ribeirão Preto, SP, Brazil|Unidade de Pronto Atendimento/UPA - 13 de Maio/Dr. Luis Atílio Losi Viana (UPA Covid), Ribeirão Preto, São Paulo, Brazil
  • Study designs - Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|Primary Purpose: Treatment
  • Enrollment - 100
  • Age - 18 Years and older   (Adult, Older Adult)
  • Outcome measures - Prevention of severe/critical stage of Covid19|Time to CoVid19 symptoms relief and number of participants with negative Clinical CoVid19 symptoms as assessed by CTCAE v5.0|Change in proinflammatory cytokine concentration|Describe the parenchymal lung damage induced by COVID-19 through a qualitative analysis with chest CT|Number of participants with treatment-related adverse events as assessed by CTCAE v5.0|Time to clinical improvement with CTCAE v5.0 CoVid19 symptoms to 0|Number of participants that need hospitalisation|28-day mortality|Time to positive-to-negative saliva 2019-n-CoV RT-PCR conversion|Reduction in viral load|Brief measure for assessing generalized anxiety disorder and depression|Increment of odor detection sensitivity
NCT04686539 Synthetic CBD as a Therapy for COVID-19 Recruiting Phase 1 Jan/20/2021 Jan/01/2022
  • Alternative id - SHEBA-20-7526-HA-CTIL
  • Interventions - Drug: CBD|Drug: Placebo
  • Study type - Interventional
  • Study results - No Results Available
  • Locations - Sheba Medical Center, Tel Hashomer, Ramat Gan, Tel Aviv, Israel
  • Study designs - Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Double (Participant, Care Provider)|Primary Purpose: Treatment
  • Enrollment - 50
  • Age - 18 Years and older   (Adult, Older Adult)
  • Outcome measures - Clinical deterioration|Changes in NEWS scale|Supportive care therapies|SARS-COV2 presence|Hospitalization Days|Cytokine Levels|Hamilton Anxiety Score
NCT04997395 Feasibility of Cannabidiol for the Treatment of Long COVID Not yet recruiting Phase 2 Jan/01/2022 Dec/01/2022
  • Alternative id - BOD202102U|2021-004534-11
  • Interventions - Drug: MediCabilis Cannabis sativa 50
  • Study type - Interventional
  • Study results - No Results Available
  • Locations -
  • Study designs - Allocation: N/A|Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment
  • Enrollment - 30
  • Age - 18 Years and older   (Adult, Older Adult)
  • Outcome measures - Recruitment rate|Tolerability for the treatment of long COVID|Number of side effects|Long COVID symptoms|Fatigue|Self-reported quality of life|Pain score|Mood (anxiety)|Mood (depression)|Sleep quality|Resting heart rate (expressed as average beats per minute)|Activity levels (number of daily steps, distance walked, stairs climbed, active minutes and calories burned)|Oxygen saturation (expressed as percentage saturation)|Daily symptoms