Lymphangioleiomyomatosis (LAM) - Pipeline Insight, 2019

"Lymphangioleiomyomatosis (LAM) - Pipeline Insight, 2019" report by outlays comprehensive insights of present scenario and growth prospects across the indication. A detailed picture of the Lymphangioleiomyomatosis pipeline landscape is provided which includes the disease overview and Lymphangioleiomyomatosis treatment guidelines. The assessment part of the report embraces, in depth Lymphangioleiomyomatosis 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, Lymphangioleiomyomatosis collaborations, licensing, mergers and acquisition, funding, designations and other product related details.
Lymphangioleiomyomatosis Understanding
Lymphangioleiomyomatosis (LAM) is a multiple cystic lung disease characterized by progressive cystic destruction of the lung and lymphatic abnormalities, frequently associated with renal angiomyolipomas (AMLs). LAM is a rare progressive multisystem disorder, which occurs either sporadically or as a manifestation of tuberous sclerosis complex (TSC) and predominantly affects women of childbearing age. This specific ailment is characterized by the extent and uncontrolled growth (proliferation) of specialized cells (smooth muscle-like LAM cells) in certain organs of the body, especially lungs, kidney, and lymphatics. It imparts some associated subsets of symptoms such as, coughing and/or difficulty breathing (dyspnea), especially following periods of exercise or exertion. It is also worth mentioning here that the LAM, affected individuals may also experience complications, including the collapse of a lung or fluid accumulation around the lungs (pleural effusion). The disorder is progressive and, in some cases, may result in chronic respiratory failure. Coming to the type-specific forms of LAM, the disease is generally being occurred in two settings, and these settings include tuberous sclerosis complex (TSC-LAM) and sporadic form. LAM that occurs sporadically is called sporadic LAM, and when it occurs in association with a rare disease called tuberous sclerosis complex (TSC), it is being called TSC-LAM.
Lymphangioleiomyomatosis Pipeline Development Activities
The report provides insights into different therapeutic candidates in discovery and preclinical, phase 1, phase 2, and phase 3 stage. Drugs under development as a monotherapy or combination therapy are also included. It also analyses key players involved in LAM targeted therapeutics development with respective active and dormant or discontinued projects. LAM pipeline report covers 4 + companies. Some of the key players include AstraZeneca (Saracatinib), AI Therapeutics (LAM-001), etc.
The report is built using data and information traced from the researcher's proprietary databases, company/university websites, clinical trial registries, conferences, SEC filings, investor presentations and featured press releases from company/university web sites and industry-specific third party sources, etc.
Lymphangioleiomyomatosis Analytical Perspective by Report
• In-depth Lymphangioleiomyomatosis Commercial Assessment of products
This report provides an in-depth Commercial Assessment of therapeutic drugs have been included which comprises of collaborations, Licensing, Acquisition –Deal Value Trends. The sub-segmentation is described in the report which includes Company-Company Collaborations (Licensing / Partnering), Company-Academia Collaborations, and Acquisition analysis in both Graphical and tabulated form.
• Lymphangioleiomyomatosis Clinical Assessment of products
The report comprises of comparative clinical assessment of products by development stage, product type, route of administration, molecule type, and MOA type across this indication.
Scope of the report
• The Lymphangioleiomyomatosis report provides an overview of therapeutic pipeline activity for Lymphangioleiomyomatosis across the complete product development cycle including all clinical and non-clinical stages
• It comprises of detailed profiles of Lymphangioleiomyomatosis therapeutic products with key coverage of developmental activities including technology, collaborations, licensing, mergers and acquisition, funding, designations and other product related details
• Detailed Lymphangioleiomyomatosis Research and Development progress and trial details, results wherever available, are also included in the pipeline study
• Therapeutic assessment of the active pipeline products by development stage, product type, route of administration, molecule type, and MOA type
• Coverage of dormant and discontinued pipeline projects along with the reasons if available across Lymphangioleiomyomatosis
Reasons to Buy
• Establish a comprehensive understanding of the current pipeline scenario across Lymphangioleiomyomatosis to formulate effective R&D strategies
• Assess challenges and opportunities that influence Lymphangioleiomyomatosis R&D
• Develop strategic initiatives by understanding the focus areas of leading companies.
• Gather impartial perspective of strategies of the emerging competitors having potentially lucrative portfolio in this space and create effective counter strategies to gain competitive advantage
• Get in detail information of each product with updated information on each project along with key milestones
• Devise Lymphangioleiomyomatosis in licensing and out licensing strategies by identifying prospective partners with progressing projects for Lymphangioleiomyomatosis to enhance and expand business potential and scope
• Our extensive domain knowledge on therapy areas support the clients in decision-making process regarding their therapeutic portfolio by identifying the reason behind the inactive or discontinued drugs