Progressive Supranuclear Palsy Headed Toward Cure

Progressive supranuclear palsy (PSP) is a brain disorder which impacts vision, cognition, movement, and speech. This disease results in weakness by affecting certain parts of the brain above the cell clusters, known as nuclei (supranuclear), which are involved in controlling eye movements. It usually manifests in mid-to late adulthood, and the survival rate of people suffering from PSP is five to nine years after the disease first appears. It is also referred to as Steele–Richardson–Olszewski syndrome.

Signs and Symptoms

The signs and symptoms of PSP vary on an individual basis, and the first symptom is usually the loss of balance while walking. Patients may experience unexplained falls or stiffness in gait. With disease progression, problems in controlling eye movements and blurring of vision become the common observations. Slowing of the eye movements is the definitive clue for a proper PSP diagnosis. Alterations of mood and behavior, such as apathy and depression, are also exhibited by patients. Other symptoms of PSP are a mask-like facial expression, slowed movements, and monotone speech.

Causes

The exact cause of PSP is not yet established; the symptoms are caused by the gradual deterioration of brain cells in certain areas, specifically the brain stem. Abnormal tau protein deposits in the nerve cells are the hallmark of the disease. This protein is associated with microtubules, which help the axons transmit information through the nerves. Abnormal protein aggregates in the surrounding cells to form protein clumps, thereby spreading throughout the nervous system. Another possible theory is that of cellular damage by free radicals, which are continuously generated by cells during normal metabolism; these damage other molecules under certain circumstances.

Diagnostic Tests

There are no specific laboratory or imaging tests currently available for a definitive PSP diagnosis. It is often misdiagnosed as the symptoms are comparatively rare and similar to other movement disorders, such as Parkinson’s disease. Brain shrinkage may show on magnetic resonance imaging (MRI) scans, and a positron emission tomography (PET) scan may be used to detect early signs that may not appear on the MRI.

Treatment

No medication or surgical procedure is available for PSP currently, and the treatment is done based on the appearance of symptoms. Antiparkinsonian agents such as levodopa help in managing stiffness, slowness, and balance, but the effect is minimal and doesn’t last long. Anti-depressants are also prescribed to control excessive drooling and for pain relief, whereas botulinum injections are used for treating excessive eye closing.

PSP therapeutics Pipeline

The PSP therapeutics pipeline is witnessing growth due to the receipt of the orphan drug status by several pharmaceutical companies for their under-development drugs. A provision of the U.S. Food and Drug Administration, the Orphan Drug Act grants a special status to a biological product or drug for the treatment of a rare condition upon a sponsor’s request. Certain incentives, such as tax credits, federal grants and a waiver of the filing fees, which is mentioned in the Prescription Drug User Fee Act, are provided under this designation.

One of the drugs in the Progressive Supranuclear Palsy therapeutics pipeline is BIIB092. Being developed by Biogen Inc., it was under the Phase II development stage in November 2017. Also known as BMS-986168, it is a humanized monoclonal antibody, which works by inhibiting the tau protein. It is being developed to be administered through the intravenous route. Bristol-Myers Squibb Company gave the drug licensing rights to Biogen Inc.

Download the report sample at: https://www.pharmaproff.com/request-sample/1230

Therefore, with the entry of more companies, the pipeline would advance, hopefully finding a definitive treatment for PSP.

Ulcerative Colitis (UC) Therapeutics Pipeline to Witness Significant Growth due to Positive Clinical Results in the Coming Years

Ulcerative colitis (UC) is a disease that affects colon or large intestine and results in inflammation of the colon and development of ulcers on intestinal linings. The disease is a result of improper functioning of immune system. As a repercussion, white blood cells (WBCs) reach the lining of large intestine, resulting in its inflammation. Signs of the disease usually are cramps in abdominal region, bloody stools, lose or urgent bowel movements, and others. The disease is non-contagious. Moreover, family history is a significant risk factor for the disease.

Download the sample pages of report at: https://www.pharmaproff.com/enquiry/1252

Treatment options for UC include infliximab, tofacitinib, aminosalicylate, corticosteroid, immunosuppressant, and ciclosporin for the reduction of inflammation. Surgery is the ultimate solution for the disease in extreme cases. The diagnosis of the disease is possible through physical examination and lab tests.

Xeljanz (Pfizer Inc.), Simponi and Remicade (Janssen Biotech Inc.), and Entyvio (Takeda Pharmaceuticals Company Limited) are some of the U.S. Food and Drug Administration (USFDA) approved drugs for the treatment for UC.

Get the detailed analysis at: https://www.pharmaproff.com/report/ulcerative-colitis-pipeline-analysis

According to the research findings, majority of the pipeline drug candidates are being developed for oral administration. It has been observed that the oral route of medication is convenient, available in delayed or rapid release formulation, less risk of systemic infections, and inexpensive in nature, and also provides improved patient’s compliance. Administration of therapeutics for UC through the oral route has shown promising results in clinical studies.

Companies that are involved in developing therapeutics for UC have shown positive clinical results in various phases of drug development. For instance, GW Pharmaceuticals plc, announced positive preliminary top-line results of phase IIa trial evaluating GWP42003 extract for treatment of UC in October 2014, which revealed that patients administered with the drug showed positive effects for UC.

It has been observed that many pharmaceutical companies are developing new and improved technologies for the development of UC therapeutics. For instance, Seres Therapeutics Inc. have developed microbiome technology to design specific therapies for particular diseases. For instance, the company developed Ecobiotic drugs for the treatment of UC.

Xeljanz, Simponi, Remicade, and Entyvio are some of the approved drugs for the treatment of UC. These drugs hold significant share in the global UC therapeutics market. Therefore, with the emergence of late- and mid-stage pipeline products in the market, the overall UC therapeutics market is expected to grow significantly in the upcoming years.

Some of the key players involved in the development of UC therapeutics are Pfizer Inc., Takeda Pharmaceutical Company Limited, Seres Therapeutics Inc., Janssen Biotech Inc., Receptos Inc., EA Pharma Co. Ltd., Celgene Corporation, and InDex Pharmaceuticals AB.

UC Therapeutics Pipeline Analysis

  • By Phase
  • By Molecule Type
  • By Route of Administration
  • By Company

The report comprises detailed pipeline analysis of therapeutics being developed for the treatment of UC. Comprehensive insights on the pipeline products have been provided, with special focus on strategic developments of key players, information on drug licensing, designations, financing, and grants, technological advancements, patents, and upcoming conferences. In addition, the report highlights the winning strategies of companies involved in the UC therapeutics development. Detailed regulatory approval procedures in the U.S., Europe, and Japan are also provided in this report. Furthermore, the report contains competitive analysis and extensive information on monotherapies, combination therapies, targets and mechanisms of action, and drug origin with respect to UC.