메디채널

주메뉴 바로가기
본문 바로가기

기상청 제공

닫기

라이프

Alphamab Oncology Announces IND Application for Innovative PD-L1/αvβ6 Bispecific ADC JSKN022 was Officially Accepted by CDE

SUZHOU, China, Aug. 4, 2025 -- Alphamab Oncology (stock code: 9966.HK) announced that the Investigational New Drug (IND) application for JSKN022, an independently developed innovative bispecific antibody-drug conjugate (ADC) targeting PD-L1 and integrin αvβ6, has been officially accepted by the Center for Drug Evaluation (CDE) of the National Medical Products Administration (NMPA). The Company plans to initiate a first-in-human (FIH) clinical study of JSKN022 for the treatment of advanced malignant solid tumors. JSKN022 is an innovative bispecific ADC developed in-house with Alphamab's
- 김갑성 기자
- 2025-08-04 09:28
Alveolus Bio Secures Strategic Investment from Shilpa Medicare to Advance Groundbreaking Pulmonary Therapeutics

Shilpa Medicare Serves as Lead Investor, Positioning Alveolus Bio for Phase 2 Clinical Trials and First-in-Human Studies CAMBRIDGE, Mass. and BIRMINGHAM, Ala. and RAICHUR, India, Aug. 4, 2025 -- Alveolus Bio, a pioneering respiratory drug development biotech company founded by Dr. Vivek Lal from University of Alabama at Birmingham, AL, has announced a strategic financing round led by Shilpa Medicare Limited (BSE: 524742) (NSE: SHILPAMED), a prominent global pharmaceutical company with extensive expertise in respiratory therapeutics manufacturing and biotechnology innovation.&nb
- 김갑성 기자
- 2025-08-04 08:00
United Imaging Teases Multi-modality "Provider Success" Product Launches at AHRA 2025

The newly FDA-cleared uMR® Ultra and the uOmniscan™ are the first major announcements leading into the AHRA Annual Meeting in Las Vegas. HOUSTON, Aug. 4, 2025 -- United Imaging, a global manufacturer of modern medical imaging technology, will again be among the largest exhibitors at AHRA 2025 in Las Vegas, the Association for Medical Imaging Management, with a very hands-on, interactive display of new software and hardware technology. Building on examples of how it helps healthcare providers be successful, the company will showcase its breadth and scale across 85 countries (
- 김갑성 기자
- 2025-08-04 00:22
First Subject Enrolled in Phase 1 Clinical Trial for Luye Pharma's Investigational Antidepressant Targeting NET/DAT/GABAAR

SHANGHAI, Aug. 3, 2025 -- Luye Pharma Group today announced that the first subject has been enrolled in a Phase 1 clinical trial in China for its LY03021, which was filed through China's Class 1 pathway for innovative drugs. LY03021 is an inhibitor of the norepinephrine transporter (NET), the dopamine transporter (DAT), and a gamma-aminobutyric acid type A receptor-positive allosteric modulator (GABAAR PAM), intended for the treatment of Major Depressive Disorder (MDD). MDD has a high prevalence rate, a high disability rate, and a high recurrence rate. In China, the lifetime prevalence
- 김갑성 기자
- 2025-08-03 18:23
Mabwell Announces IND Application Acceptance for CDH17-Targeting ADC 7MW4911 from Both NMPA and FDA

SHANGHAI, Aug. 1, 2025 -- Mabwell (688062.SH), an innovative biopharmaceutical company with entire industry chain, announced that its proprietary CDH17-targeting antibody-drug conjugate (ADC), 7MW4911, has received Investigational New Drug (IND) application acceptance from China's National Medical Products Administration (NMPA) and an IND Acknowledgement Letter from the U.S. Food and Drug Administration (FDA). 7MW4911 is an investigational CDH17-targeting ADC developed using Mabwell's proprietary IDDC™ platform. Its highly optimized structure integrates three key elements: Ma
- 김갑성 기자
- 2025-08-01 22:00
Everest Medicines Expands Strategic Investment in I-MAB

- Everest will invest US$30.9 million (equivalent to approximately HK$242.6 million) in cash in I-Mab. Inclusive of I-MAB shares already held by Everest, the pro forma ownership will be 16.1%. - I-Mab's Claudin 18.2 x 4-1BB bispecific antibody, givastomig, demonstrated an impressive overall response rate (ORR) of 83% in combination with immunotherapy in a Phase 1b trial of first line gastric cancers. - I-Mab's differentiated 4-1BB receptor targeting platform and bispecific antibody pipeline are highly complementary with the Company's existing mRNA cancer vaccines and in vivo CAR-
- 김갑성 기자
- 2025-08-01 21:02
Kazia Therapeutics Announces $2 Million Private Placement at Premium to Market

SYDNEY, Aug. 1, 2025 -- Kazia Therapeutics Limited (NASDAQ: KZIA), an oncology-focused drug development company, today announced that it has entered into a securities purchase agreement with certain established institutional investors for a private placement of equity securities (PIPE). Pursuant to the securities purchase agreement, the Company agreed to offer and sell to an aggregate of approximately $2.0 million of ordinary shares and prefunded warrants. The securities being sold in the PIPE are priced at a 5% premium to the closing price of Kazia's ADSs on July 31, 2025. The PIPE is struc
- 김갑성 기자
- 2025-08-01 20:00
2025 알츠하이머 협회 국제 콘퍼런스(AAIC), 주요 연구 성과 발표

토론토, 2025년 8월1일 -- 알츠하이머 협회 국제 콘퍼런스® 2025(Alzheimer's Association International Conference®, AAIC®)에서 발표된 최신 연구 결과들이 알츠하이머병 및 기타 치매의 위험 요인, 진단, 치료에 대한 과학적 이해를 높였다. 주요 내용은 다음과 같다. 미국 POINTER 임상시험에서 인지 기능 저하 위험이 있는 노인에게 두 가지 생활 습관 개입이 인지 능력을 향상시켰다. 특히 체계적인 지원과 책임감을 강조한 개입은 자기 주도적 개입보다 더 큰 개선 효과를 보였으며, 최대 2년간 정상적인 노화 관련 인지 기능 저하를 예방하는 데 도움이 됐다. 알츠하이머 협회는 알츠하이머병 진단에 도움을 주기 위한 전문의의 혈액 바이오마커 검사 사용에 대한 첫 번째 임상진료지침(CPG)을 발표했다. 다섯 건의 연구 데이터에 따르면, 혈압, 콜레스테롤, 당뇨병 치료에 사용되는 일반적인 약물 조합이 인지 기능 저하를 늦출 수 있는 것으로 나타났다. 60만 명 이상을 대상으로 한 연구에서 대기 중 납과 환경에 존재하는 납이 50년 후의 기억력 문제와
- 김갑성 기자
- 2025-08-01 19:52
Atombeat and BioDuro Announce Strategic Partnership to Launch an AI-Powered Platform for Accelerated Peptide Drug Discovery

SAN DIEGO, Aug. 1, 2025 -- On July 30, 2025, Atombeat Inc., a leading force in AI for drug discovery, and BioDuro, a globally trusted Contract Research, Development, and Manufacturing Organization (CRDMO), announced a strategic collaboration to an AI powered platform for accelerated peptide drug discovery. This collaboration brings together Atombeat's in silico modeling expertise, AI-accelerated & data-driven design platform with BioDuro's expertise in discovery chemistry, biology and DMPK to accelerate the development of next-generation peptides. By enabling a seamless end
- 김갑성 기자
- 2025-08-01 18:08
Energenesis Biomedical Announces Positive Phase I Results for ENERGI-F705PD, a Potential Disease-Modifying Treatment for Parkinson's Disease

[ 메디채널 김갑성 기자 ] The Phase I trial of ENERGI-F705PD tablet was a randomized, double-blind, placebo-controlled study designed to evaluate the safety, tolerability, and pharmacokinetics of the investigational drug in 24 healthy subjects. The results confirmed the favorable safety and tolerability profile of ENERGI-F705PD and successfully validated its sustained-release oral formulation. Energenesis plans to advance ENERGI-F705PD into a Phase II trial. TAIPEI, Aug. 1, 2025 -- Energenesis Biomedical Co., Ltd. (TWSE: 6657), a clinical-stage biotechnology company focused on cellular e
- 김갑성 기자
- 2025-08-01 15:52

이전

31 32 33 34 35 36 37 38 39 40

많이 본 기사

최근기사

2025-09-07_SUN

발행인 : 최희정 | 편집인 : 김갑성 |
등록번호: 서울특별시 아53302 | 등록일 2020-09-25 | 전화번호 02-565-7119 |
주소 : 서울특별시 강남구 영동대로 602, 6층 E115 (삼성동)
Copyright @메디채널 Corp. All rights reserved.

UPDATE: 2025년 09월 07일 19시 40분