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Myelofibrosis Pipeline Analysis report 2019 (H1) covers more than 10 drugs currently in different phases of development. Myelofibrosis is a chronic serious disorder which disrupts the normal production of the blood cells due to the excessive scarring in the bone marrow and belongs to a group of diseases called myeloproliferative disorders. The exac
Myelodysplastic Syndromes (MDS) are conditions that can occur when the blood cells in the bone marrow become abnormal. It is considered as a type of cancer. Myelodysplastic syndromes affect hematopoiesis at the stem cell level, as indicated by cytogenetic abnormalities, molecular mutations, and morphologic and physiologic abnormalities in mutation and differentiation of one or more of the hematopoietic cell lines. The dysplastic cells in the bone marrow have
Myasthenia Gravis Pipeline Analysis report covers 17 drugs currently in different phases of development. Myasthenia gravis (MG) is a neuromuscular disorder caused by impaired communication between nerves and muscles leading to the weakness and fatigue of the skeletal muscles. Symptoms of MG include slurred anf troubled speech, problems walking and lifting of objects, facial paralysis, difficulty in breathing, swallowing and chewing, extreme fatigue and double vision. It h
Hypoparathyroidism Pipeline Analysis report covers 5 drugs currently in different phases of development. Hypoparathyroidism is a rare condition that arises due to inadequate production, secretion, and activity of the parathyroid hormone. The decreased level of parathyroid hormone leads to low calcium levels as well as low potassium levels in the bl
Congenital afibrinogenemia Pipeline Analysis report covers drugs of 2 companies currently in different phases of development. Congenital afibrinogenemia is an autosomal recessive blood coagulation disorder which is caused by mutations in one of the three genes; FGA, FGB, or FGG. Each of these genes is responsible for making a subunit of a protein (
Clostridium Difficile infections Pipeline Analysis 2018 – Focusing on Clinical Trials and Results, Drug Profiling, Patents, Collaborations, and Other Developments.Clostridium Difficile infections Pipeline Analysis report covers drugs of 37 companies currently in different phases of development. Clostridium Difficile infections are caused by a bacterium, Clostridium difficile which causes diarrho
Choroideremia Pipeline Analysis report covers 5 drugs currently in different phases of development. Choroideremia is a rare inherited disorder characterized by progressive vision loss due to degeneration of the choriocapillaris, retinal pigment epithelium, and the photoreceptor of the eye. Symptoms of the disease are night-blindness, vision loss in
Cachexia Pipeline Analysis 2018 – Focusing on Clinical Trials and Results, Drug Profiling, Patents, Collaborations, and Other Developments.Cachexia Pipeline Analysis report covers 21 drugs currently in different phases of development. Cachexia or muscle wasting is a condition characterised by extreme weight loss and muscle wasting including body fat. It generally affects the people with serious
Autoimmune Hepatitis Pipeline Analysis report covers drugs of 7 companies currently in different phases of development. Autoimmune hepatitis is a long-lasting disease in which the body’s immune system fights against the normal liver cells instead of fighting against bacteria, viruses or other foreign substances. This gives rise to the liver inflammation leading to liver damage and failure. If diagnosed early, autoimmune hepatitis can be treated vi
Alport Syndrome Pipeline Analysis report covers more than 5 drugs currently in different phases of development. Alport Syndrome is an inherited disorder involving the glomerular basement membrane of the kidney. The disease is characterized by loss of kidney function, hearing loss, and ophthalmic disorders. Symptoms of the disease are hematuria, nep
Alagille Syndrome Pipeline Analysis report covers therapies which include companies and research organizations or institutes, in total 4 in number currently in different phases of development. Alagille syndrome (ALGS) is a genetic disorder which occurs due to the mutations caused in either of the JAG1 or NOTCH2 gene. The genes instruct in making pr
Adrenoleukodystrophy is a rare genetic disorder characterised by loss or damage of myelin sheath surrounding and insulating the nerve cells. The damage of the myelin sheath further leads to the progressive loss of the fuctioning of the adrenal glands. Symptoms of adrenoleukodystrophy are muscle spasms and pain, impaired vision, trouble balancing the body, deterioration of motor control, Adrenal insufficiency and lethargy and clumsiness. Diagnosi