Source: Skye Bioscience, Inc. 10/21/2021
Skye Bioscience, Inc. (OTCQB: SKYE) (“Skye” or the “Company”), a biopharmaceutical company developing proprietary, synthetic cannabinoid-derived molecules to treat glaucoma and other diseases with significant unmet need, announced today researchers from the University of Mississippi presented two Skye-sponsored studies at the 2021 American Association of Pharmaceutical Scientists Meeting (AAPS) PharmSci 360 held October 17-20, 2021, in Philadelphia, Pennsylvania. The first study evaluated the intraocular pressure (IOP) lowering effects of different nanoemulsion (NE) formulations of THCVHS. The second examined the effect on IOP of co-administering THCVHS with other classes of IOP-lowering drugs.
Details of the poster presentations are as follows:
IOP Profile in Dutch Belted Rabbits Following Topical Application of ∆9-Tetrahydrocannabinol-Valine-Hemisuccinate (THC-VHS, NB1111) Nanoemulsion Formulations
- The THC and THC-VHS nanoemulsion formulations did not exhibit any significant difference (p>0.05) in terms of intensity of action, but duration of activity differed significantly (p<0.05). With THC-VHS-NEC (SBI-100), IOP remained about 20% below baseline even at 9 hours post treatment.
- Both THC-VHS-NEC and netarsudil formulations performed better than latanoprost in terms of average max drop (p<0.05) in IOP as well as duration of activity (p<0.05). However, there was no significant difference between THC-VHS-NEC and netarsudil (p>0.05) in terms of average max drop and duration of activity on IOP lowering.
Co-administration
of ∆9-Tetrahydrocannabinol-Valine-Hemisuccinate (THC-VHS, NB1111) and
Netarsudil, a Rho-Kinase Inhibitor, Produces Superior IOP Lowering
Activity in Dutch Belted Rabbits
- The THC-VHS-NEC (SBI-100) + Rhopressa® (netarsudil) combination demonstrated the most robust IOP lowering profile and was better than the THC-VHS-NEC formulation alone (p<0.05) or Rhopressa® alone (p<0.05).
- Rhopressa® + latanoprost was better (p<0.05) than latanoprost alone, but the activity was significantly less than Rhopressa® alone (p<0.05).
- Latanoprost + THC-VHS-NEC combination exhibited an IOP-lowering profile similar (p>0.05) to that of latanoprost alone.
Formulation | Avg max Drop in IOP (%) | Duration of activity (min) |
THC-VHS-NEC | 27.5±2.1 | > 5403 |
THC-VHS-NEC + Rhopressa® | 32.4±2.6 1,2 | > 5403 |
Rhopressa® | 30.6±1.4 2 | > 5403 |
Rhopressa® + latanoprost | 22.7±2.9 | 540 |
latanoprost | 21.3±2.1 | 480 |
latanoprost + THC-VHS-NEC | 21.6±2.9 | 540 |
1 statistically significant from both Rhopressa® + latanoprost, latanoprost + THC-VHS-NEC at p<0.05
2 statistically significant from latanoprost at p<0.05
3 IOP remained about 20% below baseline
“We are pleased to see Skye’s sponsored research with our collaborators at the University of Mississippi on SBI-100 be accepted and presented at a prominent scientific meeting such as AAPS - it highlights the quality of our science and reinforces our confidence in moving this drug candidate into human trials,” said Punit Dhillon, CEO & Chair. ”Our THCVHS nanoemulsion for ocular delivery continues to demonstrate superior delivery of THC into the eye resulting in meaningful reduction of IOP, while our first study to evaluate co-administration of THCVHS with currently available therapies demonstrates the potential of our drug as an option for combination.”
Full abstracts are available online at www.aaps.org. Final posters are available on Skye’s website.
Skye
recently updated its clinical development strategy and timeline for its
Phase I study, focused on safety and tolerability in 48 healthy
volunteers, which is being initiated in Q2-22 in Australia. The study
will include single ascending dose (SAD) and multiple ascending dose
(MAD) cohorts. Skye also recently submitted and had a pre-IND meeting
request scheduled for before the end of 2021. This is an important step
in filing an Investigational New Drug Application (IND), which will
allow for human trials in the US. Under the improved clinical plan, a
robust Phase 2 study will be initiated in Q4-22 in the US. This
proof-of-concept study, focusing on dose ranging and efficacy, will be a
randomized, double-masked, placebo and active pharmaceutical controlled
study in patients with glaucoma and/or ocular hypertension.
About SBI-100
SBI-100 is the proprietary topical ocular formulation of Skye’s prodrug of tetrahydrocannabinol (THC), THCVHS and is being developed to treat glaucoma. THCVHS, a synthetic molecule, was developed using rational drug design and biochemical engineering, to enable local delivery of THC into the eye, reducing the potential for systemic side effects. Additional formulation studies have lead to the proprietary topical nanoemulsion formulation containing THCVHS, referred to as SBI-100.
In
preclinical studies, SBI-100 demonstrated superior lowering of
intraocular pressure, a major risk factor related to irreversible vision
loss, compared to the standard-of-care glaucoma treatment. SBI-100 will
be the final formulation intended for use in Skye’s first-in-human
trials expected to begin in Q2-22.
About the University of Mississippi
The
University of Mississippi, the state's flagship university, is among
the elite group of R-1: Doctoral Universities - Highest Research
Activity in the Carnegie Classification. The university has a long
history of producing leaders in public service, academics, research, and
business. Its 15 academic divisions include a major medical school,
nationally recognized schools of accountancy, law and pharmacy, and an
honors college acclaimed for a blend of academic rigor, experiential
learning, and opportunities for community action. Over 50 years ago, the
university was awarded the first federal government contract to
cultivate cannabis for research.
About Skye Bioscience
Skye
Bioscience Inc. is a biopharmaceutical company unlocking the
pharmaceutical potential of cannabinoids through the development of its
proprietary cannabinoid-derived molecules to treat diseases with
significant unmet needs. The company’s lead program, SBI-100, is focused
on treating glaucoma, the world’s leading cause of irreversible
blindness. For more information, please visit: www.skyebioscience.com.
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