All About Wilson’s Disease (WD)
Disease
By admin / December 27, 2023

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...

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Understanding Warnings and Precautions for Blincyto in Cancer Treatment
acute lymphoblastic leukemia
By admin / December 27, 2023

Understanding 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....

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Retevmo : A Revolutionary Cancer Treatment
acute lymphoblastic leukemia
By admin / November 28, 2023

Retevmo : 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...

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Hope in the form of molecules: The Blincyto Breakthrough
acute lymphoblastic leukemia
By admin / November 28, 2023

Hope 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...

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T-cell Acute Lymphoblastic Leukemia: Incidence & Survival Rate
acute lymphoblastic leukemia
By admin / October 16, 2023

T-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...

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Nelarabine Combination Therapy: Relapsed T-Cell Acute Lymphoblastic Leukemia
acute lymphoblastic leukemia
By admin / September 13, 2023

Nelarabine 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...

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Efficacy of Trientine in Patients
By admin / August 29, 2023

Efficacy 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...

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Overview of Tyrosinemia Type 1: Navigating a Rare Genetic Disorder
Hereditary tyrosinemia type
By admin / August 22, 2023

Overview 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...

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Nitisinone Breakthrough: Glimmer of Hope for Type 1B Oculocutaneous Albinism
Hereditary tyrosinemia type
By admin / August 16, 2023

Nitisinone 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....

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Nitisinone: Comprehensive description of the Drug
Hereditary tyrosinemia type
By admin / August 4, 2023

Nitisinone: 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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