ข่าวประชาสัมพันธ์ Metastatic Breast Cancer+SciClone Pharmaceuticals

Menarini Group and SciClone Pharmaceuticals Announce Exclusive Sub-Licensing Collaboration to Develop and Commercialize ORSERDU(R) (Elacestrant) in China to Address Advanced or Metastatic Breast Cancer

ORSERDU is the first treatment specifically approved for patients with ER+, HER2- advanced or metastatic breast cancer tumors that harbor ESR1 mutations, representing the first innovation in endocrine therapy in nearly 20 years. ESR1 mutations are present in up to 40% of ER+, HER2- advanced or metastatic breast cancers, and are a known driver of resistance to standard endocrine therapy, making these tumors more difficult to treat. This agreement includes undisclosed upfront, milestone payments

Menarini Group Shares New Analysis from EMERALD Clinical Study of ORSERDU(R) (Elacestrant) in Metastatic Breast Cancer at ASCO 2023

ORSERDU (elacestrant) was approved by the FDA in January 2023 for estrogen receptor (ER)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or...

Menarini Group's Elacestrant Granted Priority Review by the U.S. FDA for Patients with ER+/HER2- Advanced or Metastatic Breast Cancer

Elacestrant, if approved, would be the first oral selective estrogen receptor degrader (SERD) to be available for patients suffering from 2L and 3L ER+/HER2- advanced...

Menarini Progresses Into the Clinic With MEN1611, a PI3K Inhibitor for the Treatment of HER2 Positive Metastatic Breast Cancer

Menarini Ricerche announced today the initiation of the B-PRECISE-01 clinical trial, a multicenter phase Ib study that will evaluate the safety and efficacy of MEN1611 plus...

Study Confirms That Avastin Significantly Increases Chance of Living Without Disease Progression in Metastatic Breast Cancer

- Data From Pivotal Phase III AVADO Study Presented at ASCO for the First Time Avastin (bevacizumab), significantly improves the time patients with metastatic breast cancer...

Second Phase III Study of Avastin in 1st Line Metastatic Breast Cancer Meets its Primary Endpoint

- Results of This Trial Further Confirm the Benefit Avastin Brings to Patients With Breast Cancer. Roche announced today that a phase III study in metastatic breast cancer investigating Avastin ...

ASIANET: SCICLONE'S ZADAXIN(R) THYMOSIN ALPHA 1 IS EFFECTIVE AND SAFE...

SCICLONE'S ZADAXIN(R) THYMOSIN ALPHA 1 IS EFFECTIVE AND SAFE IN THE TREATMENT OF CHRONIC HEPATITIS B, HEPATOLOGY ARTICLE REPORTS ZADAXIN RESPONSE RATES INCREASE AFTER THERAPY ENDS SAN MATEO, Calif., May 29 /PRNewswire-AsiaNet/...

ASIANET: SCHERING-PLOUGH K.K. STARTS PIVOTAL PHASE 3 HEPATITIS B STUDY

SCHERING-PLOUGH K.K. STARTS PIVOTAL PHASE 3 HEPATITIS B STUDY OF SCICLONE'S ZADAXIN(R) THYMOSIN ALPHA 1 IN JAPAN SAN MATEO, Calif., May 12 /PRNewswire/AsiaNet/ SciClone Pharmaceuticals (Nasdaq: SCLN), announced today that Schering...

ASIANET: SCICLONE OBTAINS FIRST EUROPEAN MARKETING APPROVAL AND NEW DRUG

SCICLONE OBTAINS FIRST EUROPEAN MARKETING APPROVAL AND NEW DRUG APPLICATIONFOR ZADAXIN(R) THYMOSIN ALPHA 1- DEAL POSITIONS THE COMPANY FOR A U.S. ANDPAN EUROPEAN PARTNERING ARRANGEMENT - SAN MATEO, Calif., April 21 /PRNewswire...

ASIANET: SCICLONE'S ZADAXIN(R) THYMOSIN ALPHA 1 IN COMBINATION WITH TACE IMPROVED SURVIVAL OF LIVER CANCER PATIENTS

SCICLONE'S ZADAXIN(R) THYMOSIN ALPHA 1 IN COMBINATION WITH TACE IMPROVED SURVIVAL OF LIVER CANCER PATIENTS, STUDY FINDS SAN MATEO, Calif., March 27 /PRNewswire-Asianet/ SciClone...

ASIANET: ญี่ปุ่นไฟเขียว Schering-Plough ผลิตยาต้านไวรัสตับอักเสบบีขั้น 3

บริษัท SciClone Pharmaceuticals, Inc. (SCLN)ได้ประกาศในวันนี้ว่า บริษัท Schering-Plough K.K. (SPKK) ซึ่งเป็นบริษัทในญี่ปุ่นในเครือของบริษัท Schering-Plough Corporation ได้รับการอนุมัติจากกระทรวงสาธารณสุขและสวัสดิการของญี่ปุ่น...

ASIANET: SCICLONE AND SCHERING-PLOUGH K.K. RECEIVE JAPANESE APPROVAL TO START THE PIVOTAL PHASE 3 HEPATITIS B STUDY FOR ZADAXIN (R) THYMOSIN ALPHA 1 IN JAPAN

SCICLONE AND SCHERING-PLOUGH K.K. RECEIVE JAPANESE APPROVAL TO START THE PIVOTAL PHASE 3 HEPATITIS B STUDY FOR ZADAXIN(R) THYMOSIN ALPHA 1 IN...