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Cannabidiol

Generic Name
Cannabidiol
Brand Names
Epidiolex, Sativex, Epidyolex
Drug Type
Small Molecule
Chemical Formula
C21H30O2
CAS Number
13956-29-1
Unique Ingredient Identifier
19GBJ60SN5
Background

Cannabidiol, or CBD, is one of at least 85 active cannabinoids identified within the Cannabis plant. It is a major phytocannabinoid, accounting for up to 40% of the Cannabis plant's extract, that binds to a wide variety of physiological targets of the endocannabinoid system within the body. Although the exact medical implications are currently being investigated, CBD has shown promise as a therapeutic and pharmaceutical drug target. In particular, CBD has shown promise as an analgesic, anticonvulsant, muscle relaxant, anxiolytic, antipsychotic and has shown neuroprotective, anti-inflammatory, and antioxidant activity, among other currently investigated uses . CBD's exact place within medical practice is still currently hotly debated, however as the body of evidence grows and legislation changes to reflect its wide-spread use, public and medical opinion have changed significantly with regards to its usefulness in a number of medical conditions ranging from anxiety to epilepsy.

From a pharmacological perspective, Cannabis' (and CBD's) diverse receptor profile explains its potential application for such a wide variety of medical conditions. Cannabis contains more than 400 different chemical compounds, of which 61 are considered cannabinoids, a class of compounds that act upon endogenous cannabinoid receptors of the body . Cannabinoid receptors are utilized endogenously by the body through the endocannabinoid system, which includes a group of lipid proteins, enzymes, and receptors that are involved in many physiological processes. Through its modulation of neurotransmitter release, the endocannabinoid system regulates cognition, pain sensation, appetite, memory, sleep, immune function, and mood among many other bodily systems. These effects are largely mediated through two members of the G-protein coupled receptor family, cannabinoid receptors 1 and 2 (CB1 and CB2). CB1 receptors are found in both the central and peripheral nervous systems, with the majority of receptors localized to the hippocampus and amygdala of the brain. Physiological effects of using cannabis make sense in the context of its receptor activity as the hippocampus and amygdala are primarily involved with regulation of memory, fear, and emotion. In contrast, CB2 receptors are mainly found peripherally in immune cells, lymphoid tissue, and peripheral nerve terminals .

Tetrahydrocannabinol (THC) and cannabidiol (CBD) are two types of cannabinoids found naturally in the resin of the marijuana plant, both of which interact with the cannabinoid receptors that are found throughout the body. Although THC and CBD have been the most studied cannabinoids, there are many others identified to date including cannabinol (CBN), cannabigerol (CBG), Cannabidivarin (CBDV), and Tetrahydrocannabivarin (THCV) that can be found within the medical cannabis . While both CBD and THC are used for medicinal purposes, they have different receptor activity, function, and physiological effects. If not provided in their activated form (such as through synthetic forms of THC like Dronabinol or Nabilone), THC and CBD are obtained through conversion from their precursors, tetrahydrocannabinolic acid-A (THCA-A) and cannabidiolic acid (CBDA), through decarboxylation reactions. This can be achieved through heating, smoking, vaporization, or baking of dried unfertilized female cannabis flowers.

The primary psychoactive component of Cannabis, delta 9-tetrahydrocannabinol (Δ9-THC), demonstrates its effects through weak partial agonist activity at Cannabinoid-1 (CB1R) and Cannabinoid-2 (CB2R) receptors. This activity results in the well-known effects of smoking cannabis such as increased appetite, reduced pain, and changes in emotional and cognitive processes. In contrast to THC's weak agonist activity, CBD has been shown to act as a negative allosteric modulator of the cannabinoid CB1 receptor, the most abundant G-Protein Coupled Receptor (GPCR) in the body . Allosteric regulation is achieved through the modulation of receptor activity on a functionally distinct site from the agonist or antagonist binding site which is clinically significant as direct agonists (such as THC) are limited by their psychomimetic effects such as changes to mood, memory, and anxiety.

In addition to the well-known activity on CB1 and CB2 receptors, there is further evidence that CBD also activates 5-HT1A/2A/3A serotonergic and TRPV1–2 vanilloid receptors, antagonizes alpha-1 adrenergic and µ-opioid receptors, inhibits synaptosomal uptake of noradrenaline, dopamine, serotonin and gamma-aminobutyric acid (GABA), and cellular uptake of anandamide, acts on mitochondria Ca2+ stores, blocks low-voltage-activated (T-type) Ca2+ channels, stimulates activity of the inhibitory glycine-receptor, and inhibits activity of fatty amide hydrolase (FAAH) .

CBD is currently available in Canada within a 1:1 formulation with tetrahydrocannbinol (THC) (as the formulation known as "nabiximols") as the brand name product Sativex. It is approved for use as adjunctive treatment for symptomatic relief of spasticity in adult patients with multiple sclerosis (MS). Sativex was also given a conditional Notice of Compliance (NOC/c) for use as adjunctive treatment for the symptomatic relief of neuropathic pain in adult patients with multiple sclerosis and as adjunctive analgesic treatment for moderate to severe pain in adult patients with advanced cancer .

In April 2018, a Food and Drug Administration advisory panel unanimously recommended approval of Epidiolex (cannabidiol oral solution) for the treatment of two rare forms of epilepsy - Lennox-Gastaut syndrome and Dravet syndrome, which are among the two most difficult types of epilepsy to treat . Epidiolex was granted Orphan Drug designation as well as Fast Track Approval from the FDA for further study in these hard to treat conditions. Notably, phase 3 clinical trials of Epidiolex have demonstrated clinically significant improvement in Lennox-Gastaut syndrome and Dravet syndrome . On June 25th, 2018, Epidiolex was approved by the FDA to be the first CBD-based product available on the US market.

Indication

When used in combination with delta-9-tetrahydrocannabinol as the product Sativex, cannabidiol was given a standard marketing authorization (ie. a Notice of Compliance (NOC)) by Health Canada for the following indications:

1) as adjunctive treatment for symptomatic relief of spasticity in adult patients with multiple sclerosis (MS) who have not responded adequately to other therapy and who demonstrate meaningful improvement during an initial trial of therapy ;

Due to the need for confirmatory studies to verify the clinical benefit coupled with the promising nature of the clinical evidence, Sativex was also given a Notice of Compliance with Conditions (NOC/c) by Health Canada for the following indications:

1) as adjunctive treatment for the symptomatic relief of neuropathic pain in adult patients with multiple sclerosis;

2) as adjunctive analgesic treatment in adult patients with advanced cancer who experience moderate to severe pain during the highest tolerated dose of strong opioid therapy for persistent background pain .

Associated Conditions
Multiple Sclerosis, Seizures, Severe Pain, Moderate Pain

Jazz Pharmaceuticals Reports Strong Q1 2025 Performance with $898 Million in Revenue, Advances Pipeline with Zepzelca sNDA Submission

• Jazz Pharmaceuticals reported total revenues of $898 million in Q1 2025, with Xywav and Epidiolex showing strong year-over-year growth of 9% and 10% respectively. • The company submitted a supplemental New Drug Application for Zepzelca in combination with atezolizumab as maintenance therapy for first-line extensive-stage small cell lung cancer, based on promising Phase 3 trial results. • Jazz completed the acquisition of Chimerix, adding dordaviprone to its late-stage pipeline for H3 K27M-mutant diffuse glioma, with an FDA PDUFA target date of August 18, 2025.

New Phospholipid Complex Boosts CBD Bioavailability for Epilepsy and MS Treatment

• University of South Australia researchers have developed a phospholipid complex that increases cannabidiol solubility by up to six times, significantly enhancing its absorption in the gastrointestinal tract. • The breakthrough formulation showed 67.1% dissolution in water within three hours and 32.7% higher permeability through intestinal walls compared to unmodified CBD, potentially reducing required dosages and side effects. • Unlike traditional CBD formulations that degrade when exposed to heat, light, or oxygen, the new CBD-PLC maintained stability over 12 months of testing under varied storage conditions, making it more reliable for pharmaceutical applications.

Jazz Pharmaceuticals to Acquire Chimerix for $935M, Gaining Novel Brain Tumor Drug Candidate

• Jazz Pharmaceuticals announces acquisition of Chimerix for $935 million, gaining dordaviprone, a first-in-class treatment for rare H3 K27M-mutant diffuse glioma with FDA Priority Review status. • The FDA has set a PDUFA target action date of August 18, 2025, for dordaviprone, which could become the first approved therapy for this rare brain tumor affecting children and young adults. • The acquisition strengthens Jazz's oncology portfolio and addresses an urgent unmet need, with potential commercial launch in late 2025 and patent protection extending to 2037.

Major Pharmaceutical Companies Advance Novel Seizure Treatments with Promising Pipeline Developments

• Leading pharmaceutical companies including GSK, Eisai, and Novartis are developing innovative seizure treatments focusing on personalized medicine and targeted therapies for improved patient outcomes. • Recent FDA approval of Ztalmy in 2024 marks a breakthrough as the first treatment specifically for seizures associated with CDKL5 deficiency disorder in patients over 2 years old. • Promising pipeline candidates including Cannabidiol Oral Solution, RWJ-333369, and Retigabine demonstrate diverse therapeutic approaches targeting different neurological mechanisms for seizure control.

Harmony Biosciences Reports Strong Q4 2024 Results, Outlines Pipeline Milestones for 2025

• Harmony Biosciences achieves robust Q4 2024 financial performance with $201.27M in revenue and non-GAAP adjusted earnings of $1.08 per share, exceeding analyst expectations. • The company anticipates key clinical milestones in 2025, including Phase 3 data readout for ZYN002 in Fragile X syndrome in Q3, potentially offering the first approved treatment for this condition. • Harmony plans to initiate Phase 3 trials for next-generation Pitolisant HD formulation in narcolepsy and idiopathic hypersomnia, aiming to extend the franchise through the 2040s.

NHS Approves Fenfluramine for Children with Lennox-Gastaut Syndrome, Offering New Hope for Severe Epilepsy Treatment

• The NHS has approved fenfluramine, the first non-cannabis based treatment for Lennox-Gastaut syndrome (LGS), offering new hope for children aged 2 and above with this severe form of epilepsy. • Clinical trials demonstrated that fenfluramine reduces drop seizure frequency by 26.5% on average, with over 25% of patients experiencing a 50% or greater reduction in seizures. • The treatment will be fast-tracked through NHS England's Innovative Medicines Fund, making it available three months earlier for eligible patients who cannot tolerate existing cannabis-based treatments.

DSM-Firmenich's Solid CBD Formulation Matches Epidiolex's Bioavailability in Clinical Study

• DSM-Firmenich's CBtru, a solid CBD formulation, demonstrates comparable absorption to Jazz Pharmaceuticals' liquid Epidiolex in a 32-person clinical trial, marking a significant breakthrough in CBD drug delivery. • The novel powder formulation achieves enhanced bioavailability and higher drug loading, potentially overcoming traditional CBD absorption challenges that typically limit bioavailability to as low as 6%. • The development opens new possibilities for oral solid dosage forms of CBD, offering patients more convenient alternatives to liquid formulations while maintaining consistent drug uptake regardless of food intake.

Ananda Pharma Achieves GMP Manufacturing Milestone for MRX1 Pain Treatment Program

• Ananda Pharma has completed GMP-certified manufacturing for MRX1, advancing its development program for chemotherapy-induced peripheral neuropathy and endometriosis pain treatment. • Clinical trials are set to commence at Edinburgh University and in Australia, with the program including CIPN studies, endometriosis evaluation, and a Phase I pharmacokinetic study. • The company is proceeding with ethics submissions and MHRA regulatory discussions, aiming to secure necessary approvals for global licensing pathways including FDA and EMA.

Fragile X Syndrome Market Set for $83.2M Growth with Novel Therapeutic Approaches

• The US and German Fragile X Syndrome (FXS) market is projected to experience substantial growth of $83.2 million between 2025-2030, driven by the anticipated approval of Zygel and zatolmilast. • Combined diagnosed FXS cases in the US and Germany are expected to rise from 69,942 in 2020 to 73,216 in 2030, with a 0.47% annual growth rate. • Novel therapeutics targeting FXS pathogenesis through endocannabinoid system and cAMP signaling regulation show promise, with 73.3% of pipeline agents in early development phases.

DeFloria's AJA001: A Novel Botanical Drug for Autism Spectrum Disorder Advances to Phase 2 Trials

• DeFloria, a joint venture involving Charlotte's Web, is developing AJA001, a multi-cannabinoid botanical drug, for treating Autism Spectrum Disorder (ASD). • AJA001 has completed Phase 1 trials, demonstrating safety and a favorable pharmacokinetic profile, paving the way for Phase 2 studies. • The Phase 2 trials, planned for the second quarter of 2025, will evaluate AJA001's efficacy in children, adolescents, and adults with ASD. • AJA001 represents a unique approach as the first oral systemic full-spectrum botanical drug to navigate the FDA approval process.

Biogen and Stoke Therapeutics Collaborate to Advance Zorevunersen for Dravet Syndrome

• Biogen and Stoke Therapeutics will collaborate to develop and commercialize zorevunersen for Dravet syndrome outside the U.S., Canada, and Mexico. • Stoke's Phase 3 EMPEROR study of zorevunersen, expected to begin in mid-2025, aims to reduce seizure frequency and improve cognition and behavior in children with Dravet syndrome. • Zorevunersen, an antisense oligonucleotide targeting the SCN1A gene, has shown promising results in earlier trials, including an 87% median reduction in convulsive seizure frequency. • Biogen will provide Stoke with an upfront payment of $165 million, potential milestone payments up to $385 million, and tiered royalties on net sales in Biogen's territory.

FDA Approves Journavx, a Novel Non-Opioid Painkiller, Offering New Hope for Acute Pain Management

• The FDA has approved Journavx (suzetrigine), a first-in-class non-opioid analgesic, for treating moderate to severe acute pain in adults, offering a safer alternative to opioids. • Journavx works by selectively blocking pain signals in the peripheral nervous system, reducing pain without the addictive potential and severe side effects associated with opioids. • Clinical trials demonstrated Journavx's effectiveness in reducing pain after surgeries, with a safety profile comparable to placebo, though it didn't outperform opioid-acetaminophen combinations. • Priced at $15.50 per pill, Journavx faces challenges in accessibility due to its higher cost compared to generic opioids, but it represents a significant step in combating the opioid crisis.

DeFloria's AJA001 Shows Promise in Phase 1 Trial for Autism Spectrum Disorder

• DeFloria's AJA001, a multi-cannabinoid botanical drug, demonstrated safety and tolerability in a Phase 1 trial involving 70 healthy volunteers. • The trial showed dose-proportional pharmacokinetics for CBD and THC, with plasma concentrations comparable to existing cannabinoid therapeutics. • AJA001's pharmacodynamic effects correlated with THC levels, supporting doses up to 660 mg/day for Phase 2 trials in ASD patients. • The company plans to submit Phase 1 data to the FDA and initiate Phase 2 trials in Q2 2025 to assess AJA001's impact on ASD symptoms.

Cardiol Therapeutics Advances CardiolRx into Phase III Trial for Recurrent Pericarditis Following Positive Phase II Results

• Cardiol Therapeutics is advancing its drug, CardiolRx, into a Phase III clinical trial (MAVERIC-3) for recurrent pericarditis after promising Phase II results. • The Phase II MAvERIC-Pilot study demonstrated sustained reductions in pericarditis pain and inflammation over 26 weeks with CardiolRx treatment. • A parallel Phase II/III trial (MAVERIC-2) will assess CardiolRx in recurrent pericarditis patients after interleukin-1 blocker therapy cessation. • Analysts maintain positive ratings for Cardiol Therapeutics, citing the potential of CardiolRx and the growing market for cardiovascular drugs.

FDA Approves Ziihera (zanidatamab-hrii) for HER2-Positive Biliary Tract Cancer

• The FDA granted accelerated approval to Ziihera (zanidatamab-hrii) for adults with previously treated, unresectable or metastatic HER2-positive biliary tract cancer (BTC). • Approval was based on a 52% objective response rate and a median duration of response of 14.9 months in the HERIZON-BTC-01 trial. • Ziihera is the first dual HER2-targeted bispecific antibody and chemotherapy-free treatment option for patients with HER2-positive BTC. • A confirmatory Phase 3 trial is ongoing to evaluate zanidatamab in combination with standard-of-care therapy versus standard-of-care therapy alone.
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