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home>US Stocks>HUTCHMED - ADR
HCM
HUTCHMED - ADRHealthcare
$14.90$-0.34 (-2.24%)in 1 year
As on 13 Nov 2026 at 02:29NASDAQ
52 Week Low: $9.7752 Week High: $16.33

HUTCHMED - ADR Share Price Today

HUTCHMED - ADR opened lower at $14.99, compared with its previous close of $15.08. In the last trading session, the stock traded between $14.81 and $15.00. It showed a downward intraday trend.

Return calculator

Time Period

An investment of $100 made 5 years ago in HUTCHMED - ADR is now worth

$ 48.79

Resulting in a loss of

$ 51.21 (51.21%)

Invest with $1

Note: Past profits do not guarantee future returns.

Analyst Overview

Buy

Rating from 1 Analysts

Buy
100%
Hold
0%
Sell
0%

Markets Today

Today's Change

$-0.18 (-1.20%)

Day High

$15.00

Day Low

$14.81

Day Open

$14.99

Prev Close

$15.08

Volume

21,870

1W Return

6.89%

1M Return

9.19%

3M Return

19.34%

6M Return

15.77%

1Y Return

-2.24%

Fundamentals

Market Cap ($ Mn)

2,599

PE Ratio

123.80

PB Ratio

1.71

PEG Ratio

0.10

ROE

42.55%

ROCE

35.96%

EPS (TTM)

-

Investment Returns

1 Week

6.89%

1 Month

9.19%

3 Months

19.34%

6 Months

15.77%

9 Months

-1.40%

Financials

Quarterly
All values in $ Mn
52.2

Mar 19
50.0

Jun 19
51.6

Mar 20
55.2

Jun 20
81.6

Mar 21
75.8

Jun 21

Updates

5Nov

HUTCHMED secures US FDA orphan drug status for AIHA treatment

HUTCHMED's sovleplenib received US FDA Orphan Drug Designation for autoimmune hemolytic anemia. This is the second US FDA ODD for sovleplenib, following one for primary immune thrombocytopenia. The drug is eligible for 7 years of US market exclusivity upon regulatory approval. NDAs for sovleplenib are under review by China's NMPA for both ITP and warm AIHA.

7 days ago
21Oct

Hutchmed closes GSK license deal, secures $110 million upfront

Hutchmed closed exclusive license deal with GSK for HMPL-A830. Secures $110 million upfront payment from GSK subsidiary. Eligible for up to $1.185 billion in milestone payments. GSK gains worldwide rights excluding Greater China regions. Hutchmed retains Phase I development responsibilities globally.

22 days ago
29Sep

Hutchmed partner AstraZeneca files US NDA for lung cancer combo

AstraZeneca submitted US NDA for ORPATHYS plus TAGRISSO combination. SAFFRON Phase III trial showed improved progression-free and overall survival. Targets MET-driven NSCLC patients progressing on EGFR-TKI therapy. Combination already approved in China and authorized in Switzerland.

1mo ago
28Sep

Hutchmed initiates global trial of KRAS-EGFR therapy HMPL-A830

Hutchmed initiated Phase Ia global trial for HMPL-A830 on September 27, 2026. First patient dosed in China on September 24, 2026. GSK holds worldwide rights excluding Greater China under September 3 agreement. HMPL-A830 targets KRAS mutations prevalent in up to 89% of pancreatic cancers.

1mo ago
24Sep

HUTCHMED to present positive Phase III lung cancer data at ESMO 2026

HUTCHMED presents positive Phase III data for savolitinib-osimertinib combo at ESMO 2026. SAFFRON global study selected for Presidential Symposium; SANOVO for Proffered Paper. Trials show significant PFS and OS improvements in EGFR-mutated NSCLC patients. Additional updates on fruquintinib and surufatinib across multiple cancer types.

1mo ago
18Sep

Hutchmed H1FY26 Results: Oncology revenue rises 23% to $162 million

Oncology revenue rose 23% YoY to $162 million, driven by >40% growth in China product sales. Ex-US FRUZAQLA sales surged 70%, supporting full-year guidance of $330-$450 million. Net income stood at $16 million, excluding prior year's $460 million SHPL divestment gain. R&D expenses increased to $79 million due to AATTC clinical trials and AI investments. Cash reserves remain robust at $1.4 billion amid active collaboration discussions.

1mo ago

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