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Kelun Pharmaceutical's TROP2 ADC was approved for Phase III clinical trials for triple-negative breast cancer

 Time of Update: 2022-05-25

On April 7, Kelun Pharmaceuticals announced that the TROP2 antibody conjugated drug SKB264 (TROP2-ADC) has been approved for clinical treatment of patients with advanced or metastatic triple-negative breast cancer (TNBC) who have failed at least second-line therapy .
Phase III clinical study CheckMate -816 confirmed: preoperative use of Opdivo combined

 Time of Update: 2022-05-23

CheckMate -816 is the first phase III clinical study to demonstrate that an immune-based combination therapy can significantly improve EFS and pathological complete response (pCR) rates in patients with non-small cell lung cancer in the neoadjuvant phase .
Veru's share price surges over 180% after the success of the new crown oral drug phase III

 Time of Update: 2022-05-23

This is a randomized, double-blind, placebo-controlled Phase III clinical trial to evaluate the efficacy and safety of sabizabulin in patients with moderate-to-severe COVID-19 at risk of acute respiratory distress syndrome (ARDS) and death .
Dexmedetomidine for Bipolar Disorder-Associated Acute Agitation Phase III Positive Results Published

 Time of Update: 2022-05-23

On the key secondary endpoint, both sublingual dexmedetomidine treatment groups showed significant improvements in PEC scores as early as 20 minutes after dosing, compared with placebo .
ACC008 Phase III clinical trial completed the enrolment of clinical subjects

 Time of Update: 2022-05-21

At the same time, ACC008 completed the bioequivalence trial in March 2021, and the new drug marketing application for HIV-infected patients was accepted by NMPA in May 2021 and is currently under review .
UAE approves Phase II/III clinical trial of ReCOV sequential booster immunization

 Time of Update: 2022-05-20

On April 13, Jiangsu Recco Biotechnology Co. , Ltd. (referred to as "Recco Bio" or the "Company", stock code: 2179. HK) announced that it has obtained Arab Clinical
TauRx Alzheimer's Disease Drug Approved in China Phase III; dMed-Clinipace as Partner

 Time of Update: 2022-05-20

) of China for an Investigational New Drug Application (IND) for the study of Trx-237-801 . dMed-Clinipace, a global clinical contract research organization (CRO) headquartered in Shanghai, has been
VistaGen cooperates with Aimu Medical to complete the global Phase III clinical trial application of PH94B PALISADE

 Time of Update: 2022-05-20

>In addition to this, the companies plan to initiate the Phase 3 study in Canada, Mexico and South Korea . As an odorless, fast-acting pheromone nasal spray, PH94B has a unique potential mechanism
BASF's first-quarter sales reached 23.1 billion euros, up 19% year-on-year

 Time of Update: 2022-05-19

EBIT before special items also increased significantly in the Industrial Solutions, Materials and Nutrition & Care business areas .
The sword refers to the successful phase III clinical trial of Johnson & Johnson's Stelara Amgen biosimilar drug ABP 654!

 Time of Update: 2022-05-19

Results showed that the study met its primary efficacy endpoint: no clinically meaningful difference between ABP 654 and Stelara .
DSM sells protective materials business for more than 1.4 billion euros

 Time of Update: 2022-05-18

44 billion euros (about 10. 33 billion euros in cash .
Junshi Launches Head-to-Head Phase III Clinical Trial of New Crown Oral Drug VV116 Compared with Pfizer's Paxlovid

 Time of Update: 2022-05-18

On April 19, the website of the China Clinical Trials Registry announced a multi-center, single-blind, randomized, controlled clinical study of Junshi Bio/Wangshan Wangshui VV116 head-to-head versus Pfizer Paxlovid in the early treatment of mild to severe new coronary pneumonia .
Portuguese Port and Douro wine sales in 2021 reach record 600 million euros

 Time of Update: 2022-05-15

> of Portuguese Port and Douro wines in 2021 will reach 600 million euros, a record high; The total export value also reached 403 million euros, a year-on-year increase of 12. 4%, of which Port wine exports exceeded 330 million
WACKER sales top 2 billion euros for the first time in the first quarter of 2022, EBITDA more than doubles from the previous year

 Time of Update: 2022-05-09

>. >Driven by the above factors, the Group's EBIT also increased significantly, achieving EUR 550 million during the reporting period, more than three times that of the same period last year (EUR 166 million
Zuranolone Phase III Clinical Success for Major Depression

 Time of Update: 2022-05-01

/>>Consistent with the mechanism of GABA agonists, the main side effects of this product are drowsiness and dizziness, which are said to be nothing compared to the side effects of existing antidepressants
Express Advances Innovative Treatments for Multiple Myeloma, Sanofi and Blackstone Reach 300 Million Euro Partnership

 Time of Update: 2022-04-30

formulations of Sarclisa, Sanofi has partnered with Enable Injections, an innovator in drug delivery technology, to advance the development of subcutaneous delivery of Sarclisa with the goal of providing a unique patient-centered therapeutic experience
Weili Medical's exclusive agent product Class III medical device registration certificate was renewed and approved

 Time of Update: 2022-04-28

It is suitable for bladder urination of patients or for bladder urination and irrigation of patients after surgery, and the continuous cumulative use time does not exceed 30 days .
Sansheng Pharmaceutical's long-acting erythropoietin SSS06 project phase III clinical trial completed the first subject enrollment

 Time of Update: 2022-04-28

SHENYANG, March 16, 2022 /PRNewswire/ -- Today, 3SBio announced that the recombinant erythropoiesis-stimulating protein injection (rESP, CHO cell) (drug code: SSS06), developed by 3SBio
Exploring the role of bortezomib in newly diagnosed T-ALL/T-LL patients: a phase III COG AALL1231 clinical trial

 Time of Update: 2022-04-27

The investigators conducted a follow-up phase III trial (COG AALL1231 trial) with the primary objective of comparing random assignment to modified aBFM with/without bortezomib in T-ALL/ Event-free survival (EFS) in children and young adults with T-LL .
Preliminary analysis of safety and efficacy of ELCC 2022 sequential chemoradiotherapy followed by durvalumab in stage III NSCLC

 Time of Update: 2022-04-27

The prognosis for stage III unresectable NSCLC is always generally poor, and in 2017, the PACIFIC study improved this situation, and curative concurrent chemoradiotherapy (cCRT) followed by durvalumab consolidation therapy significantly improved patient survival .

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