XM không cung cấp dịch vụ cho cư dân của Mỹ.
R
R

Roche


Tin tức

Swiss trade surplus at CHF 4.578 bln in August

TABLE-Swiss trade surplus at CHF 4.578 bln in August Sept 19 (Reuters) - Switzerland ran a merchandise trade surplus of 4.578 billion Swiss francs in August, the Federal Customs Office said on Thursday. KEY FIGURES (millions of Swiss francs) August 2024 July 2024 Imports 15.912 19.215 Exports 20.491 24.092 Balance 4.578 4.877 The figures exclude precious metals and stones, works of art and antiques.
C
L
N
R
R
S

Swiss stocks - Factors to watch on September 19

Swiss stocks - Factors to watch on September 19 ZURICH/GDANSK, September 19 (Reuters) - Here are some of the main factors that may affect Swiss stocks on Thursday: ROCHE HOLDING AG ROG.S Roche says phase III results show Xofluza significantly reduces the transmission of influenza viruses. RICHEMONT CFR.S - 2.75 CHF/shr dividend ECONOMY Swiss August trade balance due at 0600 GMT.
A
R
R
S

Roche Says Phase III Results Show Xofluza Significantly Reduces The Transmission Of Influenza Viruses

BRIEF-Roche Says Phase III Results Show Xofluza Significantly Reduces The Transmission Of Influenza Viruses Sept 19 (Reuters) - ROCHE HOLDING AG ROG.S : POSITIVE PHASE III RESULTS SHOW XOFLUZA SIGNIFICANTLY REDUCES THE TRANSMISSION OF INFLUENZA VIRUSES DATA FROM CENTERSTONE STUDY SHOWS SINGLE-DOSE XOFLUZA REDUCES TRANSMISSION OF INFLUENZA FROM AN I
R

Vontobel assesses obesity drugs impact for Swiss insurers, med-tech companies

BUZZ-Vontobel assesses obesity drugs impact for Swiss insurers, med-tech companies ** Vontobel estimates the market potential for obesity drugs in the U.S. to reach a three-digit billion U.S. dollar amount and picks Swiss Re SRENH.S and Ypsomed YPSN.S as the most likely to profit from it ** Among Swiss life insurers, Swiss Re could benefit the most from a rising demand in life and health reinsurance, with a market share of about 15%, as obesity drugs improve life expectancy, it says ** Its posit
B
H
N
R
S
S
Z

Roche Says FDA Approves Ocrevus Zunovo™

BRIEF-Roche Says FDA Approves Ocrevus Zunovo™ Sept 16 (Reuters) - ROCHE HOLDING AG ROG.S : FDA APPROVES OCREVUS ZUNOVO™ AS THE FIRST AND ONLY TWICE-A-YEAR 10-MINUTE SUBCUTANEOUS INJECTION FOR PEOPLE WITH RELAPSING AND PROGRESSIVE MULTIPLE SCLEROSIS THIS APPROVAL IS BACKED BY A DECADE OF PROVEN SAFETY AND EFFICACY DATA OF OCREVUS® IV, WITH OVER
R

US FDA approves injectable version of Roche's multiple sclerosis therapy

UPDATE 1-US FDA approves injectable version of Roche's multiple sclerosis therapy Adds price and availability in paragraph 4 Sept 13 (Reuters) - The U.S. Food and Drug Administration on Friday approved Roche's ROG.S under-the-skin injection to treat patients with multiple sclerosis. The subcutaneous or under-the-skin therapy called Ocrevus Zunovo has the potential to expand treatment options to centers unable to administer the IV version.
B
N
R

US FDA approves injectable version of Roche's multiple sclerosis therapy

US FDA approves injectable version of Roche's multiple sclerosis therapy Sept 13 (Reuters) - The U.S. Food and Drug Administration on Friday approved Roche's ROG.S under-the-skin injection to treat patients with multiple sclerosis. The subcutaneous or under-the-skin therapy called Ocrevus Zunovo has the potential to expand treatment options to centers unable to administer the IV version.
B
N
R

FDA Approves Ocrevus Zunovo For People With Relapsing And Progressive Multiple Sclerosis

BRIEF-FDA Approves Ocrevus Zunovo For People With Relapsing And Progressive Multiple Sclerosis Sept 13 (Reuters) - Genentech: FDA APPROVES OCREVUS ZUNOVO™ AS THE FIRST AND ONLY TWICE-A-YEAR 10-MINUTE SUBCUTANEOUS INJECTION FOR PEOPLE WITH RELAPSING AND PROGRESSIVE MULTIPLE SCLEROSIS Source text for Eikon: ID:nBw29jVlta
R

Top of the Street: Roche, Fresenius, BASF, AstraZeneca, Rational, PSP Swiss Property, Swiss Prime Site

BUZZ-Top of the Street: Roche, Fresenius, BASF, AstraZeneca, Rational, PSP Swiss Property, Swiss Prime Site A round-up of notable broker activity this morning from Europe's top-ranked* analysts: ** Deutsche Bank cuts Roche ROG.S to "sell" from "buy", citing limited catalyst due to a risk of Roche creating a lot of sunk cost for little ultimate return ** J.P.Morgan upgrades Fresenius FREG.DE to "overweight" from "neutral" as it sees earnings compression at the German healthcare group coming to an
A
B
F
J
R
R
S
P
F

FDA Approves Roche’s Tecentriq Hybreza

BRIEF-FDA Approves Roche’s Tecentriq Hybreza Sept 13 (Reuters) - ROCHE HOLDING AG ROG.S : FDA APPROVES ROCHE’S TECENTRIQ HYBREZA, THE FIRST AND ONLY SUBCUTANEOUS ANTI-PD-(L)1 CANCER IMMUNOTHERAPY TECENTRIQ HYBREZA PROVIDES PATIENTS AND PHYSICIANS WITH GREATER FLEXIBILITY OF TREATMENT OPTIONS WHILE SHOWING SAFETY AND EFFICACY CONSISTENT WITH INT
R

US FDA approves injectable version of Roche's multiple sclerosis therapy

UPDATE 1-US FDA approves injectable version of Roche's multiple sclerosis therapy Adds background throughout Sept 12 (Reuters) - The U.S. Food and Drug Administration on Thursday approved Roche's ROG.S under-the-skin injection to treat patients with multiple sclerosis. The therapy is already approved as an infusion or IV therapy for multiple sclerosis, which is given twice a year, under the brand name Ocrevus.
B
N
R

US FDA approves injectable version of Roche's multiple sclerosis therapy

UPDATE 1-US FDA approves injectable version of Roche's multiple sclerosis therapy Adds background throughout Sept 12 (Reuters) - The U.S. Food and Drug Administration on Thursday approved Roche's ROG.S under-the-skin injection to treat patients with multiple sclerosis. The therapy is already approved as an infusion or IV therapy for multiple sclerosis, which is given twice a year, under the brand name Ocrevus.
B
N
R

US FDA approves injectable version of Roche's multiple sclerosis therapy

US FDA approves injectable version of Roche's multiple sclerosis therapy Sept 12 (Reuters) - The U.S. Food and Drug Administration on Thursday approved Roche's ROG.S under-the-skin injection to treat patients with multiple sclerosis. Reporting by Urvi Dugar; Editing by Subhranshu Sahu
R

FDA Approves Genentech’S Tecentriq Hybreza, The First And Only Subcutaneous Anti-Pd-(L)1 Cancer Immunotherapy

BRIEF-FDA Approves Genentech’S Tecentriq Hybreza, The First And Only Subcutaneous Anti-Pd-(L)1 Cancer Immunotherapy Sept 12 (Reuters) - Roche Holding AG ROG.S : FDA APPROVES GENENTECH’S TECENTRIQ HYBREZA, THE FIRST AND ONLY SUBCUTANEOUS ANTI-PD-(L)1 CANCER IMMUNOTHERAPY ROCHE HOLDING AG - FDA APPROVES GENENTECH'S TECENTRIQ HYBREZA FOR SUBCUTANE
R

FDA Approves atezolizumab And hyaluronidase-tqjs For Subcutaneous Injection

BRIEF-FDA Approves atezolizumab And hyaluronidase-tqjs For Subcutaneous Injection Sept 12 (Reuters) - FDA: FDA APPROVES ATEZOLIZUMAB AND HYALURONIDASE-TQJS FOR SUBCUTANEOUS INJECTION
R

Roche shares knocked by concern over side effects in obesity pill trial

UPDATE 1-Roche shares knocked by concern over side effects in obesity pill trial Roche shares fall 3.5% Early study trial showed high rate of temporary side effects JP Morgan analysts say heart rate increase is as a concern Roche plans slower ramp-up of pill dose in next trial Updates share price in paragraph 2, further details on side effects in pill trial in paragraphs 6 and 8 FRANKFURT, Sept 12 (Reuters) - Shares in Roche ROG.S dropped to a two-month low on Thursday after an experimental weig
J
P
R

Roche shares drop on side effects result in early-stage obesity pill trial

Roche shares drop on side effects result in early-stage obesity pill trial FRANKFURT, Sept 12 (Reuters) - Shares in Roche ROG.S fell on Thursday after an early-stage obesity pill candidate that carries high market hopes was linked to a high rate of temporary side effects in its initial test phase on humans. Roche shares were down 4% at the open at 0700 GMT after the company presented late on Wednesday details on the trial .
P
R

Roche slides on side effects concerns for its weigh-loss pill

BUZZ-Roche slides on side effects concerns for its weigh-loss pill ** Shares in Roche ROG.S drop around 4%, with analysts pointing to concerns around side effects of its experimental weight-loss pill, CT-996 ** J.P.Morgan says in a note that the CT-996 tolerability data raises questions on overall product profile, with high rates of side effects th
R

Swiss stocks - Factors to watch on September 12

Swiss stocks - Factors to watch on September 12 ZURICH/GDANSK, Sep 12(Reuters) - Here are some of the main factors that may affect Swiss stocks on Thursday: Roche ROG.S Roche said on Wednesday the promising results of an early-stage trial of its experimental weight-loss pill that bolstered its shares in July were based on just six patients, underscoring the uncertainty of the development project.
B
R
S

Roche says early-stage obesity pill results were based on just six patients

UPDATE 1-Roche says early-stage obesity pill results were based on just six patients Adds detail of trial in paragraph 6, company comment in paragraph 7, further detail in paragraphs 8-10 FRANKFURT, Sept 11 (Reuters) - Roche ROG.S said on Wednesday the promising results of an early-stage trial of its experimental weight-loss pill that bolstered its shares in July were based on just six patients, underscoring the uncertainty of the development project.
P
R



Các điều kiện

Các tài sản phổ thông

Khước từ trách nhiệm: các tổ chức thuộc XM Group chỉ cung cấp dịch vụ khớp lệnh và truy cập Trang Giao dịch trực tuyến của chúng tôi, cho phép xem và/hoặc sử dụng nội dung có trên trang này hoặc thông qua trang này, mà hoàn toàn không có mục đích thay đổi hoặc mở rộng. Việc truy cập và sử dụng như trên luôn phụ thuộc vào: (i) Các Điều kiện và Điều khoản; (ii) Các Thông báo Rủi ro; và (iii) Khước từ trách nhiệm toàn bộ. Các nội dung như vậy sẽ chỉ được cung cấp dưới dạng thông tin chung. Đặc biệt, xin lưu ý rằng các thông tin trên Trang Giao dịch trực tuyến của chúng tôi không phải là sự xúi giục, mời chào để tham gia bất cứ giao dịch nào trên các thị trường tài chính. Giao dịch các thị trường tài chính có rủi ro cao đối với vốn đầu tư của bạn.

Tất cả các tài liệu trên Trang Giao dịch trực tuyến của chúng tôi chỉ nhằm các mục đích đào tạo/cung cấp thông tin và không bao gồm - và không được coi là bao gồm - các tư vấn tài chính, đầu tư, thuế, hoặc giao dịch, hoặc là một dữ liệu về giá giao dịch của chúng tôi, hoặc là một lời chào mời, hoặc là một sự xúi giục giao dịch các sản phẩm tài chính hoặc các chương trình khuyến mãi tài chính không tự nguyện.

Tất cả nội dung của bên thứ ba, cũng như nội dung của XM như các ý kiến, tin tức, nghiên cứu, phân tích, giá cả, các thông tin khác hoặc các đường dẫn đến trang web của các bên thứ ba có trên trang web này được cung cấp với dạng "nguyên trạng", là các bình luận chung về thị trường và không phải là các tư vấn đầu tư. Với việc các nội dung đều được xây dựng với mục đích nghiên cứu đầu tư, bạn cần lưu ý và hiểu rằng các nội dung này không nhằm mục đích và không được biên soạn để tuân thủ các yêu cầu pháp lý đối với việc quảng bá nghiên cứu đầu tư này và vì vậy, được coi như là một tài liệu tiếp thị. Hãy chắc chắn rằng bạn đã đọc và hiểu Thông báo về Nghiên cứu Đầu tư không độc lập và Cảnh báo Rủi ro tại đây liên quan đến các thông tin ở trên.

Cảnh báo rủi ro: Vốn của bạn bị rủi ro. Các sản phẩm có đòn bẩy có thể không phù hợp với tất cả mọi người. Hãy xem kỹ Thông báo rủi ro của chúng tôi.