Delving into the Latest Updates on Bristol-Myers Squibb SRL with Synapse

Overview

Tags

Skin and Musculoskeletal Diseases

Otorhinolaryngologic Diseases

Other Diseases

Small molecule drug

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Technology Platform

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Disease Domain	Count

Nervous System Diseases	2
Hemic and Lymphatic Diseases	2
Endocrinology and Metabolic Disease	1
Immune System Diseases	1
Infectious Diseases	1
Neoplasms	1

Top 5 Drug Type	Count

Small molecule drug	2

Top 5 Target	Count

PBPs(Bacterial penicillin-binding protein)	1
DNA	1

这是一项非干预性上市后监测研究，旨在向中国FDA（CFDA）履行一项批准后承诺（PAC）。主要研究以盐酸达拉他韦（DCV）为基础的治疗方案在常规临床应用中用于慢性丙肝（CHC）患者的预期和非预期药物相关不良事件（AE）及严重不良事件（SAE）的发生率。

[Translation]

This is a non-interventional post-marketing surveillance study designed to fulfill a post-approval commitment (PAC) to the China FDA (CFDA). The study is focused on the incidence of expected and unexpected drug-related adverse events (AEs) and serious adverse events (SAEs) of daclatasvir hydrochloride (DCV)-based regimens in routine clinical use in patients with chronic hepatitis C (CHC).

Start Date08 May 2018

Sponsor / Collaborator

Bristol-Myers Squibb (China) Investment Co. Ltd.

[+3]

NCT03542461 / Active, not recruitingPhase 3IIT

An Open-label, Randomized Phase III Study of Early Switch Maintenance vs DElayed Second-line Nivolumab in Advanced Stage Squamous Non Small-cell Lung Cancer (NSCLC) Patients After Standard First-line Platinum-based Chemotherapy - EDEN Trial

The study's hypothesis is that using Nivolumab as early switch maintenance, after 4-6 cycles of standard first-line chemotherapy, might improve survival in patients with advanced stage squamous NSCLC.

Start Date25 Sep 2017

Sponsor / Collaborator

Bristol-Myers Squibb SRL

[+3]

CTR20132365 / RecruitingPhase 2

400mg伊马替尼治疗3个月未获得最佳响应的慢粒白血病患者中达沙替尼vs伊马替尼治疗的开放标记、随机2B期研究

[Translation] An open-label, randomized, phase 2B study of dasatinib versus imatinib in patients with chronic myeloid leukemia who have not achieved a best response to 400 mg imatinib for 3 months

本研究的主要目的是比较一线伊马替尼治疗未获得最佳反应（BCR-ABL＞10%IS），在第3个月被随机分配接受达沙替尼100mgQD或任何剂量伊马替尼治疗的患者中，一线伊马替尼第1天治疗后的12个月MMR率.

[Translation]

The primary objective of this study was to compare the 12-month MMR rate after first-line imatinib day 1 in patients who did not achieve optimal response to first-line imatinib (BCR-ABL > 10% IS) and were randomized to receive dasatinib 100 mg QD or any dose of imatinib at month 3.

Start Date08 May 2014

Sponsor / Collaborator

Bristol-Myers Squibb (China) Investment Co. Ltd.

[+3]

100 Clinical Results associated with Bristol-Myers Squibb SRL

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0 Patents (Medical) associated with Bristol-Myers Squibb SRL

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1

Literatures (Medical) associated with Bristol-Myers Squibb SRL

ClinicoEconomics and Outcomes Research

Update of the budget impact analysis of the simplification to atazanavir + ritonavir + lamivudine dual therapy of HIV-positive patients receiving atazanavir-based triple therapies in Italy starting from data of the Atlas-M trial

Article

Author: Di Giambenedetto, Simona ; Restelli, Umberto ; Fabbiani, Massimiliano ; Nappi, Carmela ; Croce, Davide

100 Deals associated with Bristol-Myers Squibb SRL

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100 Translational Medicine associated with Bristol-Myers Squibb SRL

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Pipeline

Pipeline Snapshot as of 23 Dec 2024

The statistics for drugs in the Pipeline is the current organization and its subsidiaries are counted as organizations,Early Phase 1 is incorporated into Phase 1, Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3

Approved

2

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