Expertise in
9
conditions

Kenshi Suzuki

Tokyo, JP 
Expertise in
9
conditions
Tokyo, JP 
OverviewLocationsClinical Research

Overview

Kenshi Suzuki practices in Tokyo, Japan. Suzuki is highly rated in 9 conditions, according to our data. Their top areas of expertise are Multiple Myeloma, Primary Amyloidosis, Agranulocytosis, Bone Marrow Transplant, and Tissue Biopsy.

Their clinical research consists of co-authoring 254 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years.

Locations

Tokyo, Japan
Other Locations
Japan
Shizuoka, Japan
Shibuya, 1508935, Japan
Chiba, Japan
Nagoya, 4678601, Japan
Hamamatsu, 4328561, Japan
Okazaki, Japan
Nagasaki, Japan
Kashiwa, Japan
Toyoake, Japan
Tsukuba, 3058573, Japan
Gifu-shi, Japan
Naka, 3191195, Japan
Yokohama, 2408501, Japan
Kawasaki, Japan
Wako, 3510198, Japan
Chuo, Japan

Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.

2 Clinical Trials

A Phase III, Open-Label, Randomized Study to Evaluate the Efficacy and Safety of Single Agent Belantamab Mafodotin Compared to Pomalidomide Plus Lowdose Dexamethasone (Pom/Dex) in Participants With Relapsed/Refractory Multiple Myeloma (RRMM) (DREAMM 3)
A Phase III, Open-Label, Randomized Study to Evaluate the Efficacy and Safety of Single Agent Belantamab Mafodotin Compared to Pomalidomide Plus Lowdose Dexamethasone (Pom/Dex) in Participants With Relapsed/Refractory Multiple Myeloma (RRMM) (DREAMM 3)
Enrollment Status: Active_not_recruiting
Publish Date: June 10, 2025
Intervention Type: Drug
Study Drugs: Belantamab Mafodotin, Pom/Dex (Pomalidomide plus Low Dose Dexamethasone)
Study Phase: Phase 3
A Phase I Open-Label, Dose Escalation Study to Investigate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, Immunogenicity and Clinical Activity of the Antibody Drug Conjugate GSK2857916 in Japanese Participants With Relapsed/Refractory Multiple Myeloma
A Phase I Open-Label, Dose Escalation Study to Investigate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, Immunogenicity and Clinical Activity of the Antibody Drug Conjugate GSK2857916 in Japanese Participants With Relapsed/Refractory Multiple Myeloma
Enrollment Status: Completed
Publish Date: April 10, 2025
Intervention Type: Drug
Study Drugs: Belantamab Mafodotin, Bortezomib, Dexamethasone, Pomalidomide
Study Phase: Phase 1
View 1 Less Clinical Trial

254 Total Publications

Cytomegalovirus Retinitis During Idecabtagene Vicleucel Therapy in Patients With Relapsed/Refractory Multiple Myeloma.
Cytomegalovirus Retinitis During Idecabtagene Vicleucel Therapy in Patients With Relapsed/Refractory Multiple Myeloma.
Journal: Transplant infectious disease : an official journal of the Transplantation Society
Published: February 28, 2025

Areas of Expertise

MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.

Learn more about MediFind’s expert tiers

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