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ArriVent BioPharma

15.09
-13.3700-46.98%
Pre-market: 14.93-0.1600-1.06%05:37 EDT
Volume:19.75M
Turnover:262.99M
Market Cap:744.05M
PE:-4.08
High:15.79
Open:12.09
Low:11.36
Close:28.46
52wk High:35.83
52wk Low:11.36
Shares:49.31M
Float Shares:32.11M
Volume Ratio:32.00
T/O Rate:61.52%
Dividend:- -
Dividend Rate:- -
EPS(TTM):-3.6975
EPS(LYR):-4.3239
ROE:-53.25%
ROA:-33.11%
PB:2.03
PE(LYR):-3.49

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US Research Roundup-Allstate, Caribou Biosciences, Zscaler

Reuters
·
2 hours ago

ArriVent Retains Buy Rating as Analyst Sees Upside from Broader Pipeline Despite Trial Miss, Cutting Price Target to $22

TIPRANKS
·
13 hours ago

ArriVent Biopharma price target lowered to $18 from $45 at Jefferies

TIPRANKS
·
15 hours ago

Top Midday Decliners

MT Newswires Live
·
15 hours ago

Why This Biotech Stock is Having Its Worst Day Ever

Dow Jones
·
Yesterday

Analyst Maintains Buy on ArriVent Despite Trial Setback, Trims Price Target to $15 Ahead of Key ADC Data

TIPRANKS
·
Yesterday

ArriVent BioPharma Down over 52%, on Track for Record Low Close and Record Percent Decrease

Dow Jones
·
Yesterday

Arrivent Biopharma, Inc. : Guggenheim Cuts Target Price to $18 from $45

THOMSON REUTERS
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Yesterday

ArriVent says Phase 3 firmonertinib trial did not meet endpoint

TIPRANKS
·
Yesterday

ArriVent BioPharma's Lung Cancer Drug Fails to Meet Primary Endpoint in Phase 3 Trial

Dow Jones
·
Yesterday

ArriVent Falls After Lung Cancer Drug Misses Late-Stage Trial Goal

Reuters
·
Yesterday

Arrivent Biopharma Shares Down 62.4% Premarket After Co's Lung Cancer Therapy Fails Late-Stage Trial

THOMSON REUTERS
·
Yesterday

ArriVent's Lung Cancer Treatment Fails Late-Stage Trial

Reuters
·
Yesterday

ArriVent Says Phase 3 Furvent Trial of Firmonertinib in First-Line EGFR Exon 20 Insertion NSCLC Misses Primary PFS Endpoint

Reuters
·
Yesterday

Arrivent Biopharma, Inc.: a Trend Toward an Improvement in Overall Survival was Also Observed

THOMSON REUTERS
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Yesterday

Arrivent Biopharma - Furvent Phase 3 Trial of Firmonertinib Does not Meet Primary Endpoint of Pfs by Bicr

THOMSON REUTERS
·
Yesterday

Arrivent Biopharma - Confirmed Orr by Bicr 60% for Firmonertinib 240Mg, 33% for Control

THOMSON REUTERS
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Yesterday

Arrivent Biopharma - Safety Profile in Furvent Consistent with Previous Studies, no New Safety Signals

THOMSON REUTERS
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Yesterday

Arrivent Biopharma - Clinical Benefit Observed with Secondary Endpoints Including Pfs and Confirmed Orr

THOMSON REUTERS
·
Yesterday

Arrivent Announces Program Update from the Phase 3 Furvent Trial of Firmonertinib in First-Line Egfr Exon 20 Insertion Mutant Nsclc

THOMSON REUTERS
·
Yesterday