This “Radiodermatitis - Pipeline Insight, 2021,” report provides comprehensive insights about 5+ companies and 5+ pipeline drugs in Radiodermatitis 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.
Radiodermatitis Understanding
Radiodermatitis (radiation dermatitis, radiation-induced skin reactions, or radiation injury) is a significant side effect of ionizing radiation delivered to the skin during cancer treatment as well as a result of nuclear attacks and disasters. More specifically, 95 % of cancer patients receiving radiation therapy will develop some form of radiodermatitis, including erythema, dry desquamation, and moist desquamation. These radiation skin reactions result in a myriad of complications, including delays in treatment, diminished aesthetic appeal, and reduced quality of life. Radiation-induced dermatitis can be classified as acute or chronic. Acute radiation dermatitis occurs within 90 days of exposure to radiation. The patient may have skin changes ranging from faint erythema (reddening) and desquamation (peeling skin) to skin necrosis (death of skin cells) and ulceration, depending on the severity of the reaction. The onset of chronic radiation dermatitis may occur from 15 days to 10 years or more after the beginning of radiation therapy. It is an extension of the acute process and involves further inflammatory changes in the skin. Topical corticosteroids may be prescribed for radiation dermatitis for 2 to 4 weeks. Many small studies have investigated the use of topical therapies, as either preventative agents or for management of skin reactions as they occur.
"Radiodermatitis - Pipeline Insight, 2021" report by the publisher outlays comprehensive insights of present scenario and growth prospects across the indication. A detailed picture of the Radiodermatitis pipeline landscape is provided which includes the disease overview and Radiodermatitis treatment guidelines. The assessment part of the report embraces, in depth Radiodermatitis 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, Radiodermatitis collaborations, licensing, mergers and acquisition, funding, designations and other product related details.
Report Highlights
The companies and academics are working to assess challenges and seek opportunities that could influence Radiodermatitis R&D. The therapies under development are focused on novel approaches to treat/improve Radiodermatitis.
This segment of the Radiodermatitis 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.
The MTS-01 (Tempol) drug product is a topical gel containing 4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl. The composition of MTS-01 is used for indications requiring topical applications of the lead compound. Such indications include the prevention of radiation dermatitis, psoriasis, and other inflammatory skin conditions. MTS-01 blocks inflammatory pathways. TEMPOL is a stable free radical that readily reacts with toxic oxygen species including superoxide (O2.-), hydroxyl radical (.OH), and secondary radicals produced by the oxidation of biological macromolecules, including lipid radicals. TEMPOL reaches every cell in the body and repairs damaged cellular environments thereby increasing mitochondria output and improving overall cellular function. Adamis has a worldwide license to use Tempol for the use of reducing radiation dermatitis in patients undergoing treatment for cancer. The drug is currently being evaluated in Phase III stage of development for the treatment of Radiodermatitis.
This segment of the report provides insights about the different Radiodermatitis drugs segregated based on following parameters that define the scope of the report, such as:
There are approx. 5+ key companies which are developing the therapies for Radiodermatitis. The companies which have their Radiodermatitis drug candidates in the most advanced stage, i.e. Phase III include, Adamis Pharmaceuticals.
The drugs have been categorized under various product types like Mono, Combination and Mono/Combination.
The report provides insights into different therapeutic candidates in phase II, I, preclinical and discovery stage. It also analyses Radiodermatitis therapeutic drugs key players involved in developing key drugs.
The report covers the detailed information of collaborations, acquisition and merger, licensing along with a thorough therapeutic assessment of emerging Radiodermatitis drugs.
Current Treatment Scenario and Emerging Therapies:
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Geography Covered
- Global coverage
Radiodermatitis Understanding
Radiodermatitis: Overview
Radiodermatitis (radiation dermatitis, radiation-induced skin reactions, or radiation injury) is a significant side effect of ionizing radiation delivered to the skin during cancer treatment as well as a result of nuclear attacks and disasters. More specifically, 95 % of cancer patients receiving radiation therapy will develop some form of radiodermatitis, including erythema, dry desquamation, and moist desquamation. These radiation skin reactions result in a myriad of complications, including delays in treatment, diminished aesthetic appeal, and reduced quality of life. Radiation-induced dermatitis can be classified as acute or chronic. Acute radiation dermatitis occurs within 90 days of exposure to radiation. The patient may have skin changes ranging from faint erythema (reddening) and desquamation (peeling skin) to skin necrosis (death of skin cells) and ulceration, depending on the severity of the reaction. The onset of chronic radiation dermatitis may occur from 15 days to 10 years or more after the beginning of radiation therapy. It is an extension of the acute process and involves further inflammatory changes in the skin. Topical corticosteroids may be prescribed for radiation dermatitis for 2 to 4 weeks. Many small studies have investigated the use of topical therapies, as either preventative agents or for management of skin reactions as they occur.
"Radiodermatitis - Pipeline Insight, 2021" report by the publisher outlays comprehensive insights of present scenario and growth prospects across the indication. A detailed picture of the Radiodermatitis pipeline landscape is provided which includes the disease overview and Radiodermatitis treatment guidelines. The assessment part of the report embraces, in depth Radiodermatitis 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, Radiodermatitis collaborations, licensing, mergers and acquisition, funding, designations and other product related details.
Report Highlights
The companies and academics are working to assess challenges and seek opportunities that could influence Radiodermatitis R&D. The therapies under development are focused on novel approaches to treat/improve Radiodermatitis.
Radiodermatitis Emerging Drugs Chapters
This segment of the Radiodermatitis 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.
Radiodermatitis Emerging Drugs
Tempol: Adamis Pharmaceuticals
The MTS-01 (Tempol) drug product is a topical gel containing 4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl. The composition of MTS-01 is used for indications requiring topical applications of the lead compound. Such indications include the prevention of radiation dermatitis, psoriasis, and other inflammatory skin conditions. MTS-01 blocks inflammatory pathways. TEMPOL is a stable free radical that readily reacts with toxic oxygen species including superoxide (O2.-), hydroxyl radical (.OH), and secondary radicals produced by the oxidation of biological macromolecules, including lipid radicals. TEMPOL reaches every cell in the body and repairs damaged cellular environments thereby increasing mitochondria output and improving overall cellular function. Adamis has a worldwide license to use Tempol for the use of reducing radiation dermatitis in patients undergoing treatment for cancer. The drug is currently being evaluated in Phase III stage of development for the treatment of Radiodermatitis.
Radiodermatitis: Therapeutic Assessment
This segment of the report provides insights about the different Radiodermatitis drugs segregated based on following parameters that define the scope of the report, such as:
Major Players in Radiodermatitis
There are approx. 5+ key companies which are developing the therapies for Radiodermatitis. The companies which have their Radiodermatitis drug candidates in the most advanced stage, i.e. Phase III include, Adamis Pharmaceuticals.
Phases
This report covers around 5+ 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
Radiodermatitis pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as
- Oral
- Parenteral
- Intravenous
- Subcutaneous
- Topical.
- Molecule Type
Products have been categorized under various Molecule types such as
- Monoclonal Antibody
- Peptides
- Polymer
- Small molecule
- Gene therapy
- Product Type
The drugs have been categorized under various product types like Mono, Combination and Mono/Combination.
Radiodermatitis: Pipeline Development Activities
The report provides insights into different therapeutic candidates in phase II, I, preclinical and discovery stage. It also analyses Radiodermatitis 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 Radiodermatitis drugs.
Radiodermatitis Report Insights
- Radiodermatitis Pipeline Analysis
- Therapeutic Assessment
- Unmet Needs
- Impact of Drugs
Radiodermatitis Report Assessment
- Pipeline Product Profiles
- Therapeutic Assessment
- Pipeline Assessment
- Inactive drugs assessment
- Unmet Needs
Key Questions Answered
Current Treatment Scenario and Emerging Therapies:
- How many companies are developing Radiodermatitis drugs?
- How many Radiodermatitis drugs are developed by each company?
- How many emerging drugs are in mid-stage, and late-stage of development for the treatment of Radiodermatitis?
- What are the key collaborations (Industry-Industry, Industry-Academia), Mergers and acquisitions, licensing activities related to the Radiodermatitis 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 Radiodermatitis and their status?
- What are the key designations that have been granted to the emerging drugs?
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Table of Contents
IntroductionExecutive Summary
Radiodermatitis: Overview
- Causes
- Mechanism of Action
- Signs and Symptoms
- Diagnosis
- Disease Management
Pipeline Therapeutics
- Comparative Analysis
Therapeutic Assessment
- Assessment by Product Type
- Assessment by Stage and Product Type
- Assessment by Route of Administration
- Assessment by Stage and Route of Administration
- Assessment by Molecule Type
- Assessment by Stage and Molecule Type
Late Stage Products (Phase III)
- Comparative Analysis
Tempol: Adamis Pharmaceuticals
- Product Description
- Research and Development
- Product Development Activities
Mid Stage Products (Phase II)
- Comparative Analysis
Granexin gel: FirstString Research
- Product Description
- Research and Development
- Product Development Activities
Early stage products (Phase I/II)
- Comparative Analysis
LUT014: Lutris Pharma
- Product Description
- Research and Development
- Product Development Activities
Inactive Products
- Comparative Analysis
Radiodermatitis Key Companies
Radiodermatitis Key Products
Radiodermatitis- Unmet Needs
Radiodermatitis- Market Drivers and Barriers
Radiodermatitis- Future Perspectives and Conclusion
Radiodermatitis Analyst Views
Radiodermatitis Key Companies
AppendixList of Tables
Table 1 Total Products for Radiodermatitis
Table 2 Late Stage Products
Table 3 Mid Stage Products
Table 4 Early Stage Products
Table 5 Pre-clinical & Discovery Stage Products
Table 6 Assessment by Product Type
Table 7 Assessment by Stage and Product Type
Table 8 Assessment by Route of Administration
Table 9 Assessment by Stage and Route of Administration
Table 10 Assessment by Molecule Type
Table 11 Assessment by Stage and Molecule Type
Table 12 Inactive ProductsList of Figures
Figure 1 Total Products for Radiodermatitis
Figure 2 Late Stage Products
Figure 3 Mid Stage Products
Figure 4 Early Stage Products
Figure 5 Preclinical and Discovery Stage Products
Figure 6 Assessment by Product Type
Figure 7 Assessment by Stage and Product Type
Figure 8 Assessment by Route of Administration
Figure 9 Assessment by Stage and Route of Administration
Figure 10 Assessment by Molecule Type
Figure 11 Assessment by Stage and Molecule Type
Figure 12 Inactive Products
Companies Mentioned
A selection of companies mentioned in this report includes:
- Lutris Pharma
- Enveric Bio Co.
- FirstString Research
- Devonian health group Inc.
- Adamis Pharmaceuticals
- Perpetuum CropScience BV