Prof. Ash Wechalekar, Consultant Haematologist & Professor of Medicine and Haematology
Prof. Ash Wechalekar
Consultant Haematologist & Professor of Medicine and Haematology
Prof. Ash Wechalekar MD FRCP FRCPath DM
Consultant Haematologist & Professor of Medicine and Haematology
Prof. Ash Wechalekar
Consultant Haematologist & Professor of Medicine and Haematology MD FRCP FRCPath DM
Prof. Wechalekar is a Consultant Haematologist & Professor of Medicine and Haematology
Areas of expertise
- Bone marrow transplant
- CAR-T therapy
- Immunotherapy
- Monoclonal gammopathy of undetermined significance (MGUS)
- Myeloma
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Address
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HCA UK at University College Hospital
Grafton Way Building, 1 Grafton Way, London, WC1E 6AG
About Prof. Ash Wechalekar
Prof. Ashutosh Wechalekar is an internationally renowned Consultant Haematologist who specialises in plasma cell disorders, with a focus on MGUS, multiple myeloma, monoclonal protein-related disorders (MGRS), and all types of amyloidosis.
He is part of the largest UK myeloma service at University College London Hospitals (UCLH) and leads Haematology at the National Amyloidosis Centre based at the Royal Free Hospital. Additionally, he is the lead for the AL amyloidosis treatment programme. Prof. Wechalekar also serves as the Director of the laboratory at the National Amyloidosis Centre.
Prof. Wechalekar is highly active in clinical research, developing a trials network in the UK for AL amyloidosis and acting as Principal Investigator or Chief Investigator on numerous myeloma clinical trials. His work is widely published both nationally and internationally in these areas.
Areas of expertise
- Amyloidosis
- Blood cancer
- Bone marrow tests & biopsies
- Bone marrow transplant
- CAR-T therapy
- Immunotherapy
- Monoclonal gammopathy of undetermined significance (MGUS)
- Myeloma
- Waldenstrom’s macroglobulinaemia
Professional memberships
Articles by Prof. Ash Wechalekar
Disease progression in cardiac transthyretin amyloidosis is indicated by serial calculation of national amyloidosis centre transthyretin amyloidosis stage
Eight novel loci implicate shared genetic etiology in multiple myeloma, al amyloidosis, and monoclonal gammopathy of unknown significance
Minimal residual disease negativity by next-generation flow cytometry is associated with improved organ response in al amyloidosis
Preclinical toxicology and safety pharmacology of the first-in-class gadd45β/mkk7 inhibitor and clinical candidate, dtp3
Outcomes of 44 patients with newly diagnosed systemic light-chain amyloidosis associated with deletion 17p
Extracardiac 18f-florbetapir imaging in patients with systemic amyloidosis: more than hearts and minds
The amyloidosis forum: a public private partnership to advance drug development in al amyloidosis
Echocardiographic phenotype and prognosis in transthyretin cardiac amyloidosis
Deferred autologous stem cell transplantation in systemic al amyloidosis
