CHF278.50
2.89% yesterday
SIX Swiss Exchange, Apr 03, 05:31 pm CET
ISIN
CH0012032048
Symbol
ROG
Index
Sector
Industry

Roche Stock News

Neutral
Business Wire
about 9 hours ago
SOUTH SAN FRANCISCO, Calif.--(BUSINESS WIRE)--Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), announced today that new data were presented at the AD/PD 2025 International Conference on Alzheimer's and Parkinson's Diseases in Vienna, Austria. Highlights included presentations from the ongoing trontinemab Phase Ib/IIa Brainshuttle™ AD study demonstrating dose-dependent rapid ...
Neutral
GlobeNewsWire
about 9 hours ago
Basel, 3 April 2025 - Roche (SIX: RO, ROG; OTCQX: RHHBY) announced today that new data were presented at the AD/PD 2025 International Conference on Alzheimer's and Parkinson's Diseases in Vienna, Austria. Highlights included presentations from the ongoing trontinemab Phase Ib/IIa Brainshuttle™ AD study demonstrating dose-dependent rapid amyloid depletion from the brain and the potential of the ...
Neutral
CNBC
about 12 hours ago
Pharmaceutical companies breathed a sigh of relief Wednesday after U.S. President Donald Trump revealed that they would not be subject to reciprocal tariffs — but that reprieve could prove fleeting. The Trump administration is considering a so-called 232 investigation into pharmaceuticals, which could lead to import duties, according to a Bloomberg report.
AD HOC NEWS
one day ago
Die US-Bank JPMorgan hat Roche CH0012032048 nach einem Forschungsrückschlag mit dem hochdosiertem Multiple-Sklerose-Mittel Ocrevus beim Kursziel von 230 Franken auf "Underweight" belassen.
Negative
Reuters
one day ago
Roche said on Wednesday that a trial testing higher doses of its multiple sclerosis drug Ocrevus did not show an efficacy benefit over the standard dose, a setback in a bid to further boost usage of the best-selling therapy.
Neutral
GlobeNewsWire
one day ago
Basel, 02 April 2025 - Roche (SIX: RO, ROG; OTCQX: RHHBY) announced today that the Phase III MUSETTE trial comparing a high dose of OCREVUS® (ocrelizumab) intravenous (IV) infusion to the currently approved OCREVUS IV 600 mg dose in people with relapsing multiple sclerosis (RMS) did not meet its primary endpoint in showing additional benefit in slowing disability progression, as measured by a c...
Neutral
Business Wire
one day ago
SOUTH SAN FRANCISCO, Calif.--(BUSINESS WIRE)--Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), announced today that the Phase III MUSETTE trial comparing a high dose of Ocrevus® (ocrelizumab) intravenous (IV) infusion to the currently approved Ocrevus IV 600 mg dose in people with relapsing multiple sclerosis (RMS) did not meet its primary endpoint in showing additional bene...
Neutral
PRNewsWire
one day ago
Providers in the United States may now order the FDA-cleared HPV self-collection solution for their patients to use in their offices or other healthcare settings, with goal to reduce barriers to screening by enabling discreet self-collection Quest also plans to make self-collection option available at its 2,000 patient service centers in the United States early next month, expanding access to s...
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