HCMHUTCHMED (China) Ltd

Nasdaq hutch-med.com


$ 17.33 $ 0.08 (0.49 %)    

Monday, 09-Sep-2024 15:18:41 EDT
QQQ $ 452.46 $ -0.07 (-0.02 %)
DIA $ 408.61 $ 1.28 (0.31 %)
SPY $ 545.14 $ 0.47 (0.09 %)
TLT $ 100.04 $ 0.66 (0.66 %)
GLD $ 231.36 $ 0.10 (0.04 %)
$ 17.38
$ 17.25
$ 17.33 x 104
$ 17.35 x 100
$ 17.25 - $ 17.35
$ 11.93 - $ 21.92
42,452
na
3.03B
$ 1.21
$ 30.05
TBD
na
na ($ 0.00)
na
TBD na
How to Read 10-K & 10-Q Reports To View SEC Filing Reports, Please Register or Sign In
# Filing Date Period End Date Type Report Link
No Data found
Guide for Analyst Ratings To View Analyst Ratings, Please Register or Sign In
# Date Analyst Firm Upside/Downside Price Target Change Rating Change Current Rating

News

OPINIONS

 hutchmed-withdrawn-its-supplemental-new-drug-application-for-fruquintinib-application-for-advanced-gastric-cancer-in-china-following-nmpa-discussions

This supplemental NDA for fruquintinib was based on data from the Phase III FRUTIGA study, which was declared positive due to a...

 hutchmed-scores-us-success-with-cancer-drug-but-profits-still-dip

Key Takeaways: Hutchmed’s U.S. sales jumped nearly 53% in the second quarter from the previous three months, boosted by upta...

 goldman-sachs-maintains-neutral-on-hutchmed-china-raises-price-target-to-19

Goldman Sachs analyst Paul Choi maintains HUTCHMED (China) (NASDAQ:HCM) with a Neutral and raises the price target from $17 ...

 hutchmed-china-h1-eps-015-down-from-097-yoy-sales-30568m-down-from-53287m-yoy

HUTCHMED (China) (NASDAQ:HCM) reported quarterly earnings of $0.15 per share. This is a 84.54 percent decrease over earnings of...

 why-hutchmed-stock-is-moving-higher-friday

HUTCHMED announced that its New Drug Application for Tazemetostat for the treatment of relapsed or refractory follicular lympho...

Core News & Articles

− Approval Based on Results from Positive, Global, Phase 3 FRESCO-2 Trial− FRUZAQLA (fruquintinib) is the First Novel Targeted ...

 reported-earlier-hutchmed-publishes-phase-iii-sovleplenib-results-484-response-rate-in-itp-patients-versus-0-in-placebo-group

— Publication shows treatment demonstrated durable response rate of 48.4% vs. 0% with placebo —   — Presentations at EHA showc...

 reported-earlier-hutchmed-begins-phase-i-clinical-trial-of-menin-inhibitor-hmpl-506-for-hematological-malignancies-in-china

This is a Phase I, multicenter, open-label clinical study to evaluate the safety, pharmacokinetics and efficacy of HMPL-506 in ...

 hutchmed-to-present-new-and-updated-data-from-several-studies-of-compounds-discovered-at-asco-2024

Results will be presented from the registration Phase II study of fruquintinib combined with sintilimab in 98 second-line or ab...

 reported-earlier-hutchmed-to-present-sovleplenib-phase-iii-eslim-01-study-and-hematological-malignancy-programs-data-at-the-upcoming-eha2024-congress

HUTCHMED (China) Limited ("HUTCHMED") (Nasdaq/AIM:HCM; HKEX:13) today announces that topline and subgroup results from ...

 reported-earlier-hutchmed-initiates-the-raphael-registrational-phase-iii-trial-of-hmpl-306-for-patients-with-idh1--andor-idh2-mutated-relapsedrefractory-acute-myeloid-leukemia-in-china

HMPL-306 is a novel dual-inhibitor of IDH1 and IDH2 enzymes. Mutations of IDH1 and IDH2 have been implicated as drivers of cert...

 reported-earlier-hutchmed-initiates-phase-iiiii-trial-of-the-combination-of-surufatinib-and-camrelizumab-for-treatment-nave-pancreatic-ductal-adenocarcinoma-in-collaboration-with-hengrui

Almost half a million people diagnosed each year across the globe — Collaboration based on synergistic potential of inhibiti...

Core News & Articles

— If approved in the European Union, fruquintinib will be the first novel targeted therapy for metastatic colorectal cancer reg...

 hutchmed-says-initial-preclinical-data-for-hmpl-506-novel-highly-potent-and-differentiated-menin-mll-inhibitor-for-the-treatment-of-certain-types-of-acute-leukemia-at-aacr-congress-2024

Initial preclinical data will be presented for HMPL-506, a novel, highly potent and differentiated menin-MLL inhibitor for the ...

Core News & Articles

— NDA accepted and both fruquintinib and sintilimab granted Priority Review, following Breakthrough Therapy designation in July...

Core News & Articles

HUTCHMED (China) Limited ("HUTCHMED") (Nasdaq/AIM:​HCM; HKEX:​13) today announces that the supplemental New Drug Applic...

CLASS ACTION DEADLINES - JOIN NOW!

NEW CASE INVESTIGATION