IHL’s psilocybin treatment takes 2 steps forward, with a boost from the FDA and ethics approval to commence trials at Monash University

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The world-first treatment is on track to commence clinical trials in early 2022.

Across its extensive product suite, clinical stage pharmaceutical development company Incannex Healthcare (IHL:ASX) is developing a unique psilocybin therapy for the treatment of generalised anxiety disorder (GAD).

And the company announced two more key updates that further solidified its development pathway this morning, ahead of clinical trials scheduled to start early next year.

 

Ethics approval

The Phase 2a trial for IHL’s Psi-GAD treatment is being led by Dr Paul Liknaitzky, Head of Clinical Psychedelic Research at Monash University and also a member of IHL’s scientific advisory board.

On a global level, it will mark the first clinical trial examining the safety and effectiveness of psilocybin in the treatment of GAD. It’s also the largest psychedelic trial in Australia to-date.

On that front, IHL took a critical step forward this morning with confirmation the trial had received approval to proceed from the Monash University Human Research Ethics Committee (MUHREC).

The project also achieved another world-first; approval for trial therapists to take psilocybin under supportive conditions as part of their training.

The move is based on research which suggests there may be “substantial benefits” to the trial process where therapists have experience with the treatment, Liknaitzky said.

With approval now achieved, the research team will commence the drug importation process and complete the training program for therapists, before patient recruitment kicks off in early 2022.

 

Pre-IND meeting with the FDA

Along with ethics approval for the trial, IHL also received positive feedback from US health regulators following the submission of its pre-investigational new drug (pre-IND) application.

In response, the FDA “confirmed that the therapeutic strategy for the development of a psilocybin-assisted therapy for GAD is appropriate, and conveyed interest in its development”.

The FDA also provided guidance on what will be required in a long-term drug development strategy, with the goal of achieving full approval and marketing authorisation.

As part of the feedback response, crucial information was provided which will inform how IHL constructs the parameters of its Phase 2b trial, following either interim or full results from the Phase 2a trial.

The successful application IHL submitted included an overview of the Psi-GAD program, and answers to specific questions as part of an “investigational new drug (‘IND’) folder required to conduct human trials, in pursuit of FDA marketing approval in the USA”, the company said.

As it moves towards the clinical trial process, momentum is building for IHL’s world-first treatment which is also has a major market opportunity.

The project is comparable to projects such as those run by MindMed Inc and Compass Pathways, both of which are listed on the Nasdaq. Incannex is also pursuing its own Nasdaq listing after recently submitting its registration document with the US financial regulator.

Research indicates that around 3% of adults in the US and Australia suffer from GAD in any 12-month period.

That equates to an addressable market of around 9m people in the US, around 1m people in Australia.

This article was developed in collaboration with Incannex, a Stockhead advertiser at the time of publishing.

This article does not constitute financial product advice. You should consider obtaining independent advice before making any financial decisions.

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Incannex Healthcare moves forward with soft gel capsule design for IHL-42X to treat obstructive sleep apnoea

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Cannabinoid and psychedelic biotech company Incannex Healthcare (ASX: IHL) has engaged Colombian-based manufacturer Procaps S.A. to develop a soft gel capsule form of its IHL-42X cannabinoid drug for the treatment of obstructive sleep apnoea.

The pharmaceutical-grade capsules will be used for Incannex’s Phase 2, Phase 3 and open label clinical trials of IHL-42X.

Development will be supported by Procaps’ intellectual property portfolio which provides access to a range of proprietary formulation and manufacturing techniques for the finished product, including its patented Unigel technology for encapsulating solid dosage forms within capsules.

Incannex managing director Joel Latham said he was pleased to be partnering with a “sophisticated pharmaceutical company” capable of supplying clinical trials and quickly ramping up production for commercial supply.

Phase 2 trial

Incannex is currently completing a proof-of-concept Phase 2 clinical trial to assess IHL-42X, which comprises a combination of dronabinol (a man-made form of tetrahydrocannabinol) and acetazolamide.

The primary endpoint of the trial is a reduction in the apnea hypopnea index (AHI), while secondary endpoints include a reduction in the oxygen desaturation index (ODI), a reduction in daytime somnolence measured by the Epworth Sleepiness Scale (ESS) and an improvement in mood as measured by Profile of Mood States (POMS) rating scale.

Patient dosing is expected to be finalised before year end and results will be used to support an investigational new drug application with the US Food and Drug Administration (FDA).

They will also be used to inform the design of subsequent clinical trials.

In July 2021, a confidential interim analysis was performed on data from the clinical trial and the results were used to support a patent application over IHL-42X.

Incannex has also commenced a six-month open label extension to the Phase 2 trial, which seeks to re-assess the therapeutic benefit and tolerability of IHL-42X in people who have previously benefited from the drug in trials.

There is currently no registered drug remedy for sleep apnoea. The CPAP device is often prescribed however it is cumbersome, intrusive and disruptive for partners. Patient compliance to the CPAP is low so a successful pill form treatment may well be revolutionary for this condition.

Top three ranking

Procaps is the largest integrated contract development and manufacturing company in Latin America and is ranked within the top three companies globally for soft gel manufacturing capacity.

It has developed over 500 formulations for pharmaceutical and nutritional products and reached over 50 markets globally.

The company’s manufacturing plant has been approved for good manufacturing practices (GMP) by organisations including the US Food and Drug Administration, Australia’s Therapeutic Goods Administration, Health Canada and the UK’s Medicines and Healthcare Products Regulatory Agency.

This article was developed in collaboration with Incannex Healthcare, a Stockhead advertiser at the time of publishing.

This article does not constitute financial product advice. You should consider obtaining independent advice before making any financial decisions.

 

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ASX Health Stocks: Truscreen jumps 38% on business update, flagging strong growth in China

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The ASX 200 Health Index (XHJ) is up by 1.2% at the time of writing, compared to the broader index which is higher by 1%.

Truscreen Group (ASX:TRU) was the best health stock performer, up by 38% after reporting key milestones including the completion of firmware upgrades to its devices.

The upgrade is expected to provide Truscreen devices further encrypted cybersecurity and automated features, which will reduce downtime.

The company also gave the market an update on its expansion progress in China, saying that the launch of the TruScreen Made in China device has significantly expanded the addressable market in the country.

China, according to Truscreen, is its most established market and the world’s largest addressable cervical cancer market.

In Europe, the company’s push into central European countries is also gaining ground, with market access now in Serbia and Poland.  Final planning stages for trialling the clinical performance of the TruScreen device is currently underway in Poland.

The Truscreen device is a cervical cancer screening device which provides real-time, accurate detection of pre-cancerous and cancerous cervical cells in women.

Truscreen Group share price today:

 

Other ASX health stocks with notable announcements

Incannex Healthcare (ASX:IHL) +5%

The medicinal cannabis play announced that it has engaged Procaps to develop and manufacture its IHL-42X soft gel capsules.

IHL-42X is the company’s proprietary cannabinoid drug under development for the treatment of obstructive sleep apnoea.

The soft gel capsules will be pharmaceutical-grade and used in pivotal phase 2, phase 3 and open label clinical trials.

Procaps has extensive scientific expertise, and its manufacturing plant has been inspected and approved for good manufacturing practices (GMP) by multiple regulatory agencies including FDA, TGA, Health Canada and MHRA.

Incannex recently raised $18m through options exercises, ahead of its proposed Nasdaq listing.

The company is currently pursuing a US FDA approval for its range of medicinal cannabis and psychedelic products that treat anxiety and sleep disorders, traumatic brain injury, as well as lung inflammation.

Medlab Clinical (ASX:MDC) +3%

The company has sold the Australian part of its nutraceutical business, AUS Nutraceuticals, to PharmaCare, a well-established Australian health and wellness company.

Medlab will receive cash of $1.6m from PharmaCare, and will now focus completely on its core products, NanaBis and NanoCelle.

It will also look to take advantage of emerging commercial partnering opportunities after having successfully gained patents in 48 worldwide markets.

Osprey Medical (ASX:OSP) +4%

The company has experienced strong growth in Q3, with worldwide net revenue increasing by 50% on pcp to $508k.

Osprey said its strategic alliance with GE Healthcare underpinned the strong result, with an 80% increase on pcp reported for its European sales.

The company designs and manufactures proprietary devices and monitoring systems that reduce the amount of X-ray dye (contrast) used during commonly performed heart imaging procedures.

Telix Pharma (ASX:TLX) -0.34%

Telix announced that peer-reviewed results from the IPAX-1 Ph I/II study of TLX101 have been delivered in an oral presentation at the Congress of Neurological Surgeons currently taking place in Austin.

The data confirmed that the study has met its primary objective, which was to demonstrate the safety and tolerability of TLX101 at doses tested.

The results also showed overall survival of 15.97 months for patients with recurrent glioblastoma multiforme (GBM).

Doctor Care Anywhere (ASX:DOC) +0.7%

The UK-based telehealth company delivered strong growth with record revenue of £5.8 million (or around A$10.7 million) in Q3, an increase of 21.6% from the last quarter.

A record 41,000 patients had their first ever DCA (directional coronary atherectomy) consultation during the quarter, where 65% of consultations were delivered to returning patients.

DOC has reaffirmed its guidance for FY21, which is for a revenue growth of at least 100% above FY20.

Control Bionics (ASX:CBL) unchanged

The company has introduced a facility whereby Australian customers can rent CBL products.

The rental model was introduced as a number of its Australian customers had access to the CBL products delayed, as a result of the time taken to obtain funding from NDIS (National Disability Insurance Scheme).

The rental model allows customers to obtain the use of CBL products immediately, and could be rented for a minimum period of three months and a maximum period of 12 months.

CBL’s products include NeuroNode Trilogy, NeuroNode Duo, and Eye Gaze Duo – devices that help people living with paralysis and loss of speech.

Opthea Ltd (ASX:OPT) unchanged

The eye disease biotech announced that its first clinical trial sites in the Asia-Pacific region are now open for patient enrolment.

The Phase 3 trial will study its lead drug OPT-302 for the treatment of wet (neovascular) age-related macular degeneration (AMD).

Share prices today:

 

 

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Dr Boreham’s Crucible: 4 ASX stocks focused on a mind-altering $25 billion psilocybin market

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Turn on, tune in and don’t drop out. The push to develop psychedelic drugs is gaining momentum, but not quite in the way the 1960s counter-culture figure Dr Timothy Leary intended.

The late Harvard psychologist strongly advocated the use of mind-bending drugs – notably lysergic acid diethylamide (LSD) – to expand creativity and engender a general sense of well-being.

Now, the advocates are all about using psychedelics – notably 3,4-methylene-dioxy-meth-amphetamine (MDMA) and psilocybin to treat difficult conditions such as post-traumatic stress disorder (PTSD), treatment-resistant depression (TRD), general anxiety, dementia, anorexia and alcohol and nicotine addiction.

Many readers will be aware – and we’re not passing judgment – that MDMA is the party drug ecstasy, better known as molly. Psilocybin is the active component of magic mushrooms, which have long been known to put the fun into fungi.

Other mind-bending substances of interest are LSD and the horse tranquilliser ketamine (also known as the party drug Special K).

As with cannabis, these drugs have a long history of medical experimentation. LSD was first isolated by Swiss chemist Dr Albert Hofmann in 1943, after which he experienced a vivid trip on his bicycle (in more ways than one) after accidently ingesting the drug.

MDMA was first synthesised by German pharma house Merck in 1912. Meanwhile, psilocybin has long been ingested by central and south American indigenous peoples, who discovered their evening mushroom stew had a bit more zing than usual.

In the 1960s psychedelic drugs became synonymous with swingers’ “key parties” and Vietnam war protests. Serious research came to a halt after US President and moral guardian Richard Milhous Nixon (Tricky Dicky – seeing as how we’re using a lot of colloquial expressions) declared a war on drugs – a battle that has lasted much longer than the Indochina one.

As with medical (and recreational) pot, attitudes are changing – albeit slowly.

According to advocacy group Mind Medicine Australia, more than 120 psychedelic trials have been carried out in the last decade.

Mind-blowing valuations

Overseas, psychedelic drug developers are commanding, er, mind-blowing valuations. Take the $US3.2 billion market worth of the German based, Nasdaq listed Atai Life Sciences which is targeting conditions including traumatic brain injury and schizophrenia.

The private, Oxford-based Beckley Psytech raised $US80 million in August and Chicago-based venture capital group Palo Santo in July gathered $US35 million to invest in a portfolio of psychedelic stocks.

Locally, four ASX cannabis stocks have turned (expanded?) their minds to the sector: Emyria, Creso Pharma, Incannex Healthcare and Little Green Pharma.

Backed by tech entrepreneur Daniel Petrie and venture capital fund Possible Ventures, the private Sydney-based Psylo has raised $1.1 million for early research. Earlier, the Melbourne based Psychae Institute pocketed a handy $40 million from a very mysterious, unnamed American biotechnology company.

Navigating the regulatory maze

For drug development to happen in earnest, the rules need to change.

Last year, the local Therapeutic Goods Administration rejected entreaties to reschedule MDMA and psilocybin from schedule nine to schedule eight (as it did for medicinal cannabis in 2016).

Schedule nine means it’s a prohibited drug which can be used in approved clinical trials; schedule eight means it’s a controlled substance that opens the way to registration and reimbursement.

Mind Medicine Australia argued the decision was based on flawed science, including the contention that these substances were addictive.

In April this year the agency agreed to a re-think and commissioned an independent expert review (as you do).

In late September, the three-person expert committee of academics released the results of its review, which was based on a whittled-down sample of nine clinical studies on the two drugs.

To cut a long story short, the advocates seized on the committee’s headline conclusion that both drugs appeared to have “statistically significant” results, but the evidence was strongest for MDMA.

The well-tolerated substances “showed promise in highly selected populations, but only where these medicines are administered in closely supervised settings and with intensive professional support”.

Of course, the advocates weren’t suggesting otherwise. But they did gloss over the committee’s criticisms of the “variable” quality of many of the trials which, for example, included ‘blinded’ participants who appeared well-aware of what they were taking.

The Advisory Committee of Medicines Scheduling meets on November 3, with the TGA expected to announce its decision in the first week of December.

And elsewhere?

Of course, Australia is – duh – just Australia.

In the US, psychedelics were declared a banned substance in 1970, with “no currently accepted medical use”.

Official attitudes have thawed since then, to put it mildly, with the US Food and Drug Administration awarding “breakthrough” status to MDMA and psilocybin, to treat PTSD and treatment-resistant depression (TDR).

In July, the US Congress passed a law compelling the National Institute of Health to fund research into psychedelic and cannabis therapies, with an emphasis on MDMA for PTSD.

In May this year, the agency granted approval to the Multidisciplinary Association of Psychedelic Studies (MAPS) to study the use of MDMA by healthy volunteer therapists.

MAPS has completed 10 FDA-approved MDMA studies so far and is overseeing another seven.

Health Canada has a similar exemption for therapists, which points to the notion of a “guided experience” rather than users being left to pop the pills at home.

Emyria (ASX:EMD)


Share price 21 cents, market cap $32 million, 12-month share gain 162 per cent

Emyria’s work initially centred on synthetic cannabis as an alternative to the botanical stuff, which varies in quality.

The company started out its ASX life as Emerald Clinics in early 2020. The company still operates these specialist cannabis clinics, from which it gleans a useful bank of client information for its patient database.

Interestingly Emyria notes a “chronic oversupply” of cannabis, with licensed Canadian growers destroying 279,000 kilograms of the stuff in 2020.

That goes against a narrative about medical cannabis being in short supply.

But we digress and so does Emyria, which is developing a “scalable, evidence-based” clinical model for MDMA, in exclusive partnership with Mind Medicine Australia.

The crux of Emyria’s focus is a proposed phase II trial to treat PTSD with MDMA, but it appears some way from being launched.

Emyria also boasts exclusive access to a file of more than 100 MDMA analogues: a library of compounds developed by the University of Western Australia over the last decade.

Emyria is currently browsing through the library for the most useful ones, with screening to date showing “excellent purity and long-term stability.”

Emyria is executive-chaired by Dr Stewart Washer, who is also on the boards of the listed Orthocell, Cynata and Botanix.

Dr Washer and his family interests account for about 19 per cent of Emerald’s register.

Creso Pharma (ASX:CPH)


Share price 11 cents, market cap $126 million, 12-month share gain 266 per cent

Pot-stock Creso’s ASX journey since listing in 2016 has been unpredictable, to put it politely, and the wild ride continues into the psychedelic sector.

Creso had planned to merge with the Ontario based Red Light Holland, which is not a knock shop but a purveyor of “magic truffles” (psilocybin) to the legal recreational market in the Netherlands.

The new entity would have listed on the Canadian exchange under the code TRIP – and we rue we’ll never see that apt ticker.

In 2019, Creso was to have been taken over by Canadian pot play Pharma Cielo but that one didn’t get past the altar either. However, the acquisition of the smaller Canadian grower Mernova Medicinal was duly completed in 2018.

In March this year, Creso acquired Canadian outfit Halucenex, a clinical stage company focused on using psilocybin to treat PSTD, TRD and anxiety.

Halucenex is one of only three Canadian companies licensed to handle psilocybin – 10 kilograms of the stuff at any one time.

The psilocybin is synthetic: the company doesn’t forage in the fields for one of the 100-plus varieties of mushies containing the active ingredient.

Creso plans a phase II trial focused on using psilocybin for treatment-resistant PTSD. And in lieu of the Red Light Holland merger, the company is putting on its big boy’s pants for a Nasdaq listing.

Creso co-founder Dr Miri Halperin Wernli is also the president of the $US1.2 billion Mind Medicine Inc, which gives a clue about Creso’s likely hallucinogenic path.

In the meantime, the company almost doubled (cannabis derived) revenue in the first (June) half, to $3.06 million, with just over half derived from Mernova.

Incannex Healthcare (ASX:IHL)


Share price 44 cents, market cap $417 million, 12-month share gain 283 per cent

This one was formerly known as Impression Healthcare, which developed sports mouthguards under the Gameday brand.

Despite the advocacy of sports stars, it was never a scalable business and the company executed a graceful double pivot into medical cannabis and then psychedelic therapies.

On the cannabis front, Incannex is tackling conditions including traumatic brain injury, rheumatoid arthritis, irritable bowel syndrome and inflammatory lung conditions. Its most advanced program is a phase II, proof-of-concept trial targeting obstructive sleep apnoea.

On the psychedelic side, Incannex has zeroed in on the use of psilocybin for generalised anxiety disorder. The company notes that seven million Americans and one million Australians suffer moderate to severe anxiety, which makes us more neurotic than them on a per-capita basis.

Pending ethics approval, Incannex expects to launch a phase IIa trial at Monash University’s Brainpark facility.

It’s also yarning with the FDA about an investigational new drug application.

The company cites supportive studies undertaken by New York University, the University of California Los Angeles, Johns Hopkins University and London’s Imperial College.

Overall, these studies enrolled just 85 patients, with early results showing the psychedelics could be two to four times more effective as a front-line treatment relative to cognitive behavioral therapy and antidepressants.

Incannex intends to enlist 72 patients in active and placebo arms, undergoing two doses over 10 weeks. They will also undergo weekly psychotherapy sessions.

Incannex chalked up $1.9 million of revenue from cannabis oil sales in the year to June 2021 and lost $8.1 million.

As with Creso, Incannex proposes a Nasdaq listing. In mid-September its shareholders voted overwhelmingly in favor of issuing 180 million shares to facilitate an initial public offer for the listing.

Management is girded by Nasdaq listees such as Compass Pathways, which is pursuing phase II psilocybin trials for treatment-resistant depression and is valued at $US1.25 billion.

Incannex already commands a circa $400 million valuation.

Little Green Pharma (ASX:LGP)


Share price 68.5 cents, market cap $160 million, 12-month share price gain 108 per cent.

In September, Western Australia’s health mandarins granted the medicinal cannabis supplier a licence to supply psilocybin to other eligible parties to carry out research.

The company, which is backed by iron ore magnate Gina Rinehart, also said it was “well advanced in planning to sponsor a ground-breaking Perth-based clinical trial into psilocybin assisted psychotherapy”.

The research pertains to conditions including depression, post-traumatic stress disorder and anxiety.

The company reminds uninitiated folk that ‘magic mushroom’ derived psilocybin induces a psychedelic state through its action on the brain’s 5-hydroxy-tryptamine-2A serotonin receptors.

The company has also appointed Dr Stephen Bright as an adviser.

A “prominent and highly respected voice in psychedelic medicine”, Dr Bright was a co-founder of psychedelic research house Prism and a lecturer in addiction at Edith Cowan University.

“We have developed so much experience over the years through the cannabis industry and we genuinely believe we can now bring that to bear on the development of the psychedelics,” Little Green boss Fleta Solomon said.

In the meantime, Little Green will remain focused on supplying the European market with cannabis flowers and oils from its newly-acquired Danish facility.

Dr Boreham’s diagnosis:

The simple way of viewing the psychedelic therapies sector is being on the same evolutionary route of medical cannabis, but perhaps a decade behind.

Psylo co-founder Josh Ismin reportedly expects a psychedelic treatment on the market within 10 years, while others expect approval in as little as two years. But the usual experience with the FDA is that things take longer than expected, with only two cannabis-based drugs approved to date.

As with pot therapies – but even more so – the regulators appear to be largely unconvinced at this stage.

The narrative is likely to be muddied by demand from the recreational market for blue meanies, gold tops and amanitas*. And the psychedelic push is likely to confound regulatory authorities as they mull the marijuana approvals.

Still, money talks loudest and there’s no doubting the flood of investment into the sector. If the trend continues, we suspect it will be only a matter of time before the first pure-play ASX psychedelic stock emerges.

Creso cites Credence Research suggesting the market for psilocybin alone could be worth up to $US25 billion by 2025.

If such bullish sentiment endures, investors should have the trip of a lifetime.

Dr Boreham is not a qualified medical practitioner and does not possess a doctorate of any sort. *Your columnist had to look up these terms and hopefully so do you.

This column first appeared in Biotech Daily

At Stockhead, we tell it like it is. While Incannex and Creso are Stockhead advertisers, they did not sponsor this article.

The post Dr Boreham’s Crucible: 4 ASX stocks focused on a mind-altering $25 billion psilocybin market appeared first on Stockhead.

The TGA could soon relax rules on psychedelics. Here are the ASX stocks that could benefit

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After decades of being stigmatised and shunned, psychedelic drugs are making a comeback.

The Australian Therapeutic Goods Administration (TGA) has just released an independent report that found psychedelic drugs could potentially be used to treat treatment-resistant mental illnesses – when used in closely supervised clinical settings, with intensive professional support.

The independently reviewed report is TGA’s direct response to an application it received last year to enable psychedelics to be used on patients with mental illnesses.

The TGA will now assess whether it will down-schedule MDMA and psilocybin from prohibited (Schedule 9) to controlled (Schedule 8) drugs, with a decision set to be announced in December.
 

Mental illness rising globally

The TGA’s decision comes at a critical time as the world grapples with an ever-increasing rise in mental illness cases since the pandemic began.

According to a study by Harvard University, mental health disorders have risen exponentially but the development of new standard medications has not kept pace.

As a result, the study says that alternative medicines like psychedelics will grow at a robust rate of 14.5% CAGR to fill the gap, and reach a value of $6.33 billion in 2026 from $3.21 billion in 2021.

Another study conducted by Yale University on mice determined that one dose of psilocybin will immediately increase neural connections in the brains, helping it to “reorganize and adapt” to different situations.

“There’s a lot of research into how psilocybin can be used in the treatment of treatment-resistant depression, for obsessive compulsive disorder, to help people come to terms with an end-stage illness, for substance use disorders,” said the director of psychedelic research at Edith Cowan University, Dr Stephen Bright.

The US FDA has made an early move, designating MDMA as a ‘breakthrough therapy’ as early as 2017, but has so far not legalised its use beyond scientific purposes.

If the TGA does down-schedule psychedelics to a Schedule 8 (controlled drugs), it will put the drugs on par with medicinal cannabis, which has already been designated Schedule 8 in Australia since 2016.
 

ASX companies in the psychedelic space

Emyria (ASX:EMD)

The company has recently secured the rights to a University of Western Australia (UWA)’s library of more than 100 novel MDMA analogues, where the initial focus on drug discovery will be on PTSD.

Emyria is currently undergoing it first psychedelic-assisted program to assess the safety, efficacy and cost-effectiveness of MDMA-assisted psychotherapy in treating patients with PTSD.

Emyria has in the past said that substances such as psilocybin and MDMA offer a promising new approach to treating major mental illnesses that are resistant to first-line treatments.

Incannex Healthcare (ASX:IHL)

The company is currently pursuing a Phase 2a clinical trial, and developing “Psi-GAD” psilocybin therapy for Generalised Anxiety Disorder (GAD).

Incannex says around 300 million people globally are estimated to have an anxiety disorder, and GAD is often more severe and intractable than other anxiety disorders.

The Phase 2 trial will involve 72 patients to study the safety, efficacy and tolerability of psilocybin-assisted psychotherapy.

Incannex has also filed a registration statement with the US SEC as it prepares for a listing on the Nasdaq under the ticker symbol “IXHL”.

Creso Pharma Limited (ASX:CPH)

The company is one of the leading players in the psychedelic space through its Canadian subsidiary, Halucenex.

Halucenex is currently preparing a Phase 2 trial to study the efficacy of psilocybin when used for the treatment of treatment-resistant PTSD.

This follows the approval of a Controlled Drugs and Substances Dealer’s Licence granted by Health Canada back in August.

Securing the licence has made Halucenex one of only a few companies globally with the Dealer’s Licence, allowing it to work with psilocybin and other psychedelics under Health Canada’s directive.

Little Green Pharma (ASX: LGP)

The company has just received an approval from the WA Department of Health to produce the psychedelic drug being trialled in the treatment of mental illnesses such as PTSD and anxiety.

LGP has now established a special purpose subsidiary to conduct its psychedelic business, and will start manufacting psilocybin from its WA production facility.

The company is also currently engaged in extending its GMP licence to cover the psilocybin manufacture.

 

Share prices today:

 

 

 

At Stockhead we tell it like it is. While Creso Pharma and Incannex are Stockhead advertisers, they did not sponsor this article.

The post The TGA could soon relax rules on psychedelics. Here are the ASX stocks that could benefit appeared first on Stockhead.

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