This “Tourette syndrome - Pipeline Insight, 2024,” report provides comprehensive insights about 6+ companies and 6+ pipeline drugs in Tourette syndrome pipeline landscape. It covers the pipeline drug profiles, including clinical and nonclinical stage products. It also covers the therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.
Tourette syndrome - Pipeline Insight, 2024 report outlays comprehensive insights of present scenario and growth prospects across the indication. A detailed picture of the Tourette syndrome pipeline landscape is provided which includes the disease overview and Tourette syndrome treatment guidelines. The assessment part of the report embraces, in depth Tourette syndrome commercial assessment and clinical assessment of the pipeline products under development. In the report, detailed description of the drug is given which includes mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the technology, Tourette syndrome collaborations, licensing, mergers and acquisition, funding, designations and other product related details.
SCI-110: Sci Sparc SCI-110 is a unique and proprietary combination of Dronabinol, an FDA-Approved, synthetic version of delta-9-tetrahydrocannabinol (??-THC), and CannAmide™, the Company's proprietary formulation of Palmitoylethanolamide (PEA). SCI-110 is one of the innovative combinations of SciSparc cannabinoid-centric platform. Using its proprietary technology, SciSparc creates these combinations to augment the inherent properties of different cannabinoids, in this case, Dronabinol, enhancing their ability to bind with receptors in the endocannabinoid system. The potential result, as demonstrated in pre-clinical studies, is improved efficacy and in turn, lower dosage requirements and reduced side effects as compared to the cannabinoid when administered alone. In January 2022, SciSparc entered into an agreement with two clinical sites: Hannover Medical School in Hannover, Germany, and Tel-Aviv Sourasky Medical School, in Tel-Aviv, Israel, to further its Phase IIb clinical study for SCI-110, the Company's proprietary drug candidate, for patients suffering fromTourettesyndrome.
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Geography Covered
- Global coverage
Tourette syndrome Understanding
Tourette syndrome: Overview
Tourette syndrome (TS) is a hereditary neurologic movement disorder characterized by repetitive motor and vocal tics. Symptoms may include involuntary movement of the extremities, shoulders, and face accompanied by uncontrollable sounds and/or inappropriate words. Symptoms tend to be variable and follow a chronic waxing and waning course. The exact cause of Tourette syndrome isn't known, but some research suggests that it happens when there's a problem with how nerves communicate in certain areas of the brain. An upset in the balance of neurotransmitters (chemicals in the brain that carry nerve signals from cell to cell) might play a role. To be diagnosed with Tourette syndrome, a person must have several different types of tics - specifically, multiple motor tics and at least one vocal tic for at least a year. They may happen every day or from time to time throughout the year. There isn't a specific test for Tourette syndrome. Instead, the doctor looks at the family history, the medical history, and the person's symptoms to make a diagnosis. Sometimes, imaging tests like magnetic resonance imaging tests (MRIs), computerized tomography (CT) scans, electroencephalograms (EEGs), or blood tests can rule out other conditions that might cause symptoms similar to TS. The only FDA-approved medications for TS are the classical neuroleptic antipsychotic drugs, haloperidol and pimozide, which block D2 dopamine receptors.Tourette syndrome - Pipeline Insight, 2024 report outlays comprehensive insights of present scenario and growth prospects across the indication. A detailed picture of the Tourette syndrome pipeline landscape is provided which includes the disease overview and Tourette syndrome treatment guidelines. The assessment part of the report embraces, in depth Tourette syndrome commercial assessment and clinical assessment of the pipeline products under development. In the report, detailed description of the drug is given which includes mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the technology, Tourette syndrome collaborations, licensing, mergers and acquisition, funding, designations and other product related details.
Report Highlights
- In August 2021, Noema Pharma announced the initiation of its first clinical trial, a Phase IIa dose ranging study of the PDE10A inhibitor NOE-105 in Tourette syndrome. The Allevia trial is a multi-center 12-week prospective study to evaluate the safety and efficacy of once a day NOE-105, one of Noema’s extensive pipeline of products in-licensed from Roche, at a daily dose range of 5mg to15mg in adult male patients with Tourette syndrome.
- In February 2022, Asarina Pharma announced that ‘First Patient First Visit’ has taken place in its phase IIa clinical study in Tourette syndrome at Bispebjerg University Hospital, Copenhagen. The Asarina compound being trialled, Sepranolone, is an endogenous neurosteroid that has already demonstrated a strong safety profile in previous clinical studies. In preclinical studies it was found to reduce tics effectively without inducing any motor side effects.
Tourette syndrome Emerging Drugs Chapters
This segment of the Tourette syndrome report encloses its detailed analysis of various drugs in different stages of clinical development, including phase II, I, preclinical and Discovery. It also helps to understand clinical trial details, expressive pharmacological action, agreements and collaborations, and the latest news and press releases.Tourette syndrome Emerging Drugs
Ecopipam: Emalex Biosciences Unlike other Tourette syndrome treatments, which act on dopamine D2 receptors, ecopipam works by selectively blocking the actions of the D1 receptor. This mechanism may potentially reduce the likelihood of metabolic and movement disorders that have been previously linked to D2 antagonist therapy, while still treating the repetitive and compulsive behaviors associated with the disorder. Ecopipam is currently being evaluated in the Phase II D1AMOND study in children and adolescents with TS (N=150). In September 2019, the US FDA granted Fast Track designation to ecopipam for the treatment of Tourette syndrome(TS).SCI-110: Sci Sparc SCI-110 is a unique and proprietary combination of Dronabinol, an FDA-Approved, synthetic version of delta-9-tetrahydrocannabinol (??-THC), and CannAmide™, the Company's proprietary formulation of Palmitoylethanolamide (PEA). SCI-110 is one of the innovative combinations of SciSparc cannabinoid-centric platform. Using its proprietary technology, SciSparc creates these combinations to augment the inherent properties of different cannabinoids, in this case, Dronabinol, enhancing their ability to bind with receptors in the endocannabinoid system. The potential result, as demonstrated in pre-clinical studies, is improved efficacy and in turn, lower dosage requirements and reduced side effects as compared to the cannabinoid when administered alone. In January 2022, SciSparc entered into an agreement with two clinical sites: Hannover Medical School in Hannover, Germany, and Tel-Aviv Sourasky Medical School, in Tel-Aviv, Israel, to further its Phase IIb clinical study for SCI-110, the Company's proprietary drug candidate, for patients suffering fromTourettesyndrome.
Tourette syndrome: Therapeutic Assessment
This segment of the report provides insights about the different Tourette syndrome drugs segregated based on following parameters that define the scope of the report, such as:Major Players in Tourette syndrome
There are approx. 6+ key companies which are developing the therapies for Tourette syndrome. The companies which have their Tourette syndrome drug candidates in the most advanced stage, i.e. phase II include, Emalex BiosciencesPhases
This report covers around 6+ products under different phases of clinical development like- Late stage products (Phase III)
- Mid-stage products (Phase II)
- Early-stage product (Phase I) along with the details of
- Pre-clinical and Discovery stage candidates
- Discontinued & Inactive candidates
Route of Administration
Tourette syndrome pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as- Inhalation
- Inhalation/Intravenous/Oral
- Intranasal
- Intravenous
- Intravenous/ Subcutaneous
- NA
- Oral
- Oral/intranasal/subcutaneous
- Parenteral
- Subcutaneous
Molecule Type
Products have been categorized under various Molecule types such as
- Antibody
- Antisense oligonucleotides
- Immunotherapy
- Monoclonal antibody
- Peptides
- Protein
- Recombinant protein
- Small molecule
- Stem Cell
- Vaccine
Product Type
Drugs have been categorized under various product types like Mono, Combination and Mono/Combination.Tourette syndrome: Pipeline Development Activities
The report provides insights into different therapeutic candidates in phase II, I, preclinical and discovery stage. It also analyses Tourette syndrome therapeutic drugs key players involved in developing key drugs.Pipeline Development Activities
The report covers the detailed information of collaborations, acquisition and merger, licensing along with a thorough therapeutic assessment of emerging Tourette syndrome drugs.Tourette syndrome Report Insights
- Tourette syndrome Pipeline Analysis
- Therapeutic Assessment
- Unmet Needs
- Impact of Drugs
Tourette syndrome Report Assessment
- Pipeline Product Profiles
- Therapeutic Assessment
- Pipeline Assessment
- Inactive drugs assessment
- Unmet Needs
Key Questions
Current Treatment Scenario and Emerging Therapies:- How many companies are developing Tourette syndrome drugs?
- How many Tourette syndrome drugs are developed by each company?
- How many emerging drugs are in mid-stage, and late-stage of development for the treatment of Tourette syndrome?
- What are the key collaborations (Industry-Industry, Industry-Academia), Mergers and acquisitions, licensing activities related to the Tourette syndrome therapeutics?
- What are the recent trends, drug types and novel technologies developed to overcome the limitation of existing therapies?
- What are the clinical studies going on for Tourette syndrome and their status?
- What are the key designations that have been granted to the emerging drugs?
Key Players
- Emalex Biosciences
- Noema Pharma
- Asarina Pharma
- Teva Pharmaceutical
- SciSparc
- Eu MentisTherapeutics
- Synendos Therapeutics
Key Products
- Ecopipam
- NOE-105
- Sepranolone
- Deutetrabenazine
- SCI-110
- EM-221
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Table of Contents
IntroductionExecutive SummaryTourette syndrome - Analytical PerspectiveDrug profiles in the detailed report…..Drug profiles in the detailed report…..Drug profiles in the detailed report…..Drug profiles in the detailed report…..Tourette syndrome Key CompaniesTourette syndrome Key ProductsTourette syndrome- Unmet NeedsTourette syndrome- Market Drivers and BarriersTourette syndrome- Future Perspectives and ConclusionTourette syndrome Analyst ViewsTourette syndrome Key CompaniesAppendix
Tourette syndrome: Overview
Pipeline Therapeutics
Therapeutic Assessment
Late Stage Products (Phase III)
Drug Name: Company Name
Mid Stage Products (Phase II)
Ecopipam: Emalex Biosciences
Mid Stage Products (Phase II)
SCI-110: SciSparc
Preclinical and Discovery Stage Products
Drug Name: Company Name
Inactive Products
List of Tables
List of Figures
Companies Mentioned (Partial List)
A selection of companies mentioned in this report includes, but is not limited to:
- Emalex Biosciences
- Noema Pharma
- Asarina Pharma
- Teva Pharmaceutical
- SciSparc
- EuMentis Therapeutics
- Synendos Therapeutics