DelveInsight’s, “Autosomal dominant polycystic kidney disease Pipeline Insight, 2022,” report provides comprehensive insights about 12+ companies and 12+ pipeline drugs in the Autosomal dominant polycystic kidney disease 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.
Key takeaways from the Autosomal dominant polycystic kidney disease Pipeline Report
Recent Developmental Activities in the Autosomal dominant polycystic kidney disease Pipeline
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Autosomal dominant polycystic kidney disease Overview
Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disorder characterized by the formation of cysts within the kidneys. Symptoms caused by cyst formation in the kidneys include high blood pressure (hypertension), pain on the sides of the body between the last rib and the hip (flank pain), blood in the urine (hematuria) and progressively poor function of the kidneys (kidney insufficiency). In most patients, ADPKD eventually progresses to cause end stage renal disease, requiring renal replacement therapy, either dialysis or renal transplantation. ADPKD is not simply a kidney disorder and other organ systems of the body can potentially be affected (multisystem disorder) by the development of cysts. The specific symptoms present in each person depend upon the specific organ systems involved.
The liver, pancreas, a membrane covering the spinal cord and brain (arachnoid membrane), the prostate, and the glands of the male reproductive tract that produce fluid that is part of semen (seminal vesicles) may become involved. Abnormalities affecting the heart and blood vessels (cardiovascular system) may also occur in individuals with ADPKD. ADPKD usually does not become apparent until the fourth or fifth decade and was once known as “adult” polycystic kidney disease. However, it has been reported in children and infants. ADPKD is caused by mutations of one of two genes that create certain proteins essential for the proper health of the kidneys and other parts of the body. Approximately 85 % have ADPKD1, the most aggressive form of the disease; those with ADPKD2 progress to kidney insufficiency about 20 years later.
Autosomal dominant polycystic kidney disease Pipeline Insight Report
In the Autosomal dominant polycystic kidney disease pipeline report, detailed description of the drug is given which includes mechanism of action of the drug, Autosomal dominant polycystic kidney disease clinical studies, NDA approvals (if any), and product development activities comprising the technology, Autosomal dominant polycystic kidney disease collaborations, licensing, mergers and acquisition, funding, designations and other product related details.
Autosomal dominant polycystic kidney disease Emerging Drugs Profile
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Autosomal dominant polycystic kidney disease Pipeline Therapeutics Assessment
The Autosomal dominant polycystic kidney disease pipeline report proffers an integral view of the Autosomal dominant polycystic kidney disease emerging novel therapies segmented by stage, product type, molecule type, mechanism of action, and route of administration.
Scope of the Autosomal dominant polycystic kidney disease Pipeline Report
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Table of Content
Key Questions
Current Treatment Scenario and Emerging Therapies:
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