All About Wilson’s Disease (WD)
Wilson disease (also called hepatolenticular degeneration) is a rare, autosomal recessive disorder caused by abnormal copper assemblage in the body...
Read MoreUnderstanding Warnings and Precautions for Blincyto in Cancer Treatment
Blincyto, an innovative therapy for certain types of leukemia, presents significant benefits along with potential risks that necessitate careful consideration....
Read MoreRetevmo : A Revolutionary Cancer Treatment
Retevmo (Selpercatanib) is a game-changing medication in the world of oncology, offering targeted therapy for patients with specific genetic alterations...
Read MoreHope in the form of molecules: The Blincyto Breakthrough
In the realm of leukemia treatment, Blincyto emerges as a beacon of hope for both adults and children battling specific...
Read MoreT-cell Acute Lymphoblastic Leukemia: Incidence & Survival Rate
Introduction: T-cell acute lymphoblastic leukemia (T-ALL) is a specific and aggressive type of blood cancer that falls into a broader...
Read MoreNelarabine Combination Therapy: Relapsed T-Cell Acute Lymphoblastic Leukemia
T-cell acute lymphoblastic leukemia/lymphoma (T-ALL/LBL) is a challenging leukemia form mainly affecting adolescents and young adults. While initial treatments can...
Read MoreEfficacy of Trientine in Patients
Trientine is primarily used for the treatment of Wilson's disease (WD), a genetic condition/disorder that causes copper accumulation in the body. While...
Read MoreOverview of Tyrosinemia Type 1: Navigating a Rare Genetic Disorder
Dietary restrictions for phenylalanine and tyrosine are commonly recommended in addition to Nitisinone. Patients with HT-1 benefit from a reduced...
Read MoreNitisinone Breakthrough: Glimmer of Hope for Type 1B Oculocutaneous Albinism
Type 1B Oculocutaneous Albinism (OCA) is a rare genetic disorder that affects individuals' pigmentation, causing pale skin, hair, and eyes....
Read MoreNitisinone: Comprehensive description of the Drug
The FDA-approved drug nitisinone treats hereditary tyrosinemia type 1 (HT-1), a rare genetic condition that alters how the amino acid tyrosine is...
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