Ananda Scientific |
Enhanced CBD |
ANANDA’s Liquid Structure™ Enhanced CBD |
N/A (presumed oral) |
Reported as: fully water soluble (100%); high bioavailability (20× more than other CBD oils at 30 min); no degradation in stomach; stable—storable at room temperature for at least 2 years; consistent dosing—reliable results with use |
Phase 1 studies underway for indications: neuropathic pain and opioid replacement and withdrawal |
[57] |
Aphios |
APH-1501 |
Nanoencapsulated Cannabidiol Time Released Capsules; CBD encapsulated in biodegradable polymer nanospheres as a lyophilised powder |
Oral capsule |
N/A |
Phase 2 trial planned for the treatment of opioid addiction |
[58] |
Artelo Biosciences |
ART12.11 |
Co-crystal solid state formulation with TMP |
Oral |
N/A |
Pre-clinical development for PTSD, IBD, Stroke and Rare Diseases |
[59] |
Botanix Pharmaceuticals |
BTX1503 |
Gel |
Transdermal |
N/A |
Phase 1b study completed, phase 2 study underway in moderate to severe acne |
[60] |
BTX1308 |
Gel |
Transdermal |
N/A |
Phase 1b study planned in Plaque psoriasis |
[61] |
BTX1204 |
Gel |
Transdermal |
N/A |
Phase 1b study—unknown status. Phase 2 study recruiting. Indication: atopic dermatitis |
[62] |
BTX 1701 |
Facial cleanser utilising Permetrex™ skin delivery technology in conjunction with a novel oil clearing agent |
Facial cleanser |
N/A |
Small clinical study performed in mild acne |
[61] |
Columbia Care |
BeneCeed |
200 mg CBD tablet |
Oral |
N/A |
N/A |
[63] |
Diverse Biotech Inc. |
BRCX014 |
Sublingual formulation |
Sublingual |
N/A |
Two registered phase 1/2 trials in Cancer |
[64] |
Echo Pharmaceuticals |
Arvisol |
Lipophilic compound delivery technology Alitra®
|
Oral |
Claims to improve bioavailability and steadier temporal profile |
Preclinical – indicated for Rett Syndrome—Epilepsy, and Schziophrenia |
[65] |
Emerald Health Pharmaceuticals |
EHP-101 |
Synthetic CBD designed to enhance the therapeutic benefits of CBD by being a dual PPARγ and CB2 agonist |
Oral liquid |
N/A |
Phase 1 trial completed in healthy volunteers but no results published yet. Phase 2a trial registered but not yet recruiting for Diffuse Cutaneous Systemic Sclerosis |
[66] |
GW Pharmaceuticals |
GWP42003 |
NA |
i.v. |
N/A |
Phase 1 trial completed in NHIE |
[67] |
Kalytera |
K-1052 |
CBD +(S)-2-amino-(1-iminoethylamino)-5-thioheptanoic acid (iNOS inhibitor) coupled pro-drug molecule |
i.v. |
N/A |
In vivo efficacy studies in rodents completed in Sepsis-induced Acute Renal Failure and Traumatic Brain Injury |
[68] |
KAL-1816 |
CBD conjugated with naproxen |
Oral and i.v. |
N/A |
Patents filed in acute and chronic pain |
[68] |
K-1022 |
Bi-sulphate derivative of CBD |
Oral |
Water soluble |
In vivo efficacy studies performed in Ulcerative Colitis; currently ADME/PK analysis in rats, as well as non-clinical safety assessment of K-1022 in rats and dogs |
[68] |
K-1012 |
Bi-phosphate derivative of CBD; novel aerosolised formulation |
Intra-tracheally |
Soluble in aqueous solution; expected to increase the bioavailability |
In vivo efficacy studies carried out in rodents in Adult Respiratory Distress Syndrome |
[68] |
K-1032 |
L-valine-ester derivative of CBD |
Topical delivery |
N/A |
In vivo efficacy models in rodents conducted in chronic inflammatory skin diseases |
[68] |
Lexaria Bioscience Corp |
TurboCBD |
Capsules also containing American ginseng, ginkgo biloba, and organic hemp oil using DehydraTECH™ delivery technology |
Oral |
Increased circulating CBD levels compared to control CBD (+86% at 90 min) |
On the market (over the counter) |
[69,70] |
Medexus Pharmaceuticals |
CA2476833C |
Complex of RM-β-, DM-β and TM-β cyclodextrin with CBD |
N/A |
Improve aqueous solubility, dissolution rate, absorption and bioavailability |
N/A |
[71] |
Preveceutical |
Sol-Gel |
CBD gel |
Intranasal |
Expected to increase bioavailability |
Pre-clinical evidence to suggest better distribution along the olfactory epithelia |
[72] |
PureForm Global |
PureForm CBD |
Molecularly identical, non-hemp-based CBD, developed using InterMolecular Stacking Technology |
Liquid and powder |
Expected to improve solubility and stability |
N/A |
[73] |
Satipharm |
Gelpell (PLT-101) |
CBD in gelatine beads encapsulated in gastro-resistant capsules |
Oral |
30% higher bioavailability compared to oromucosal spray. |
Phase 1 and phase 2 (efficacy in paediatric epilepsy) trials completed |
[1,52] |
Vireo Health LLC |
US2019030170 |
CBD and a sulfoalkyl ether cyclodextrin |
N/A |
Increase water solubility |
N/A |
[74] |
Zynerba Pharmaceuticals |
ZygelTM ZYN002 |
Permeation-enhanced gel |
Transdermal |
N/A |
Pre-clinical, phase 1 and phase 2 trials all underway in Fragile X syndrome and other rare neuro-psychiatric conditions |
[75] |