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WVE

Wave Life Sciences Ltd.NASDAQHealthcare
$7.28+6.59%ClosedMarket Cap: $1.37B

As of 2026-04-06

Valuation

View Details

P/E (TTM)

PEG

P/B

2.49

P/S

32.08

EV/EBITDA

-3.92

DCF Value

$0.53

FCF Yield

-13.6%

Div Yield

0.0%

Margins & Returns

Gross Margin

84.5%

Operating Margin

-504.1%

Net Margin

-478.3%

ROE

-85.0%

ROA

-32.0%

ROIC

-39.0%

Financials

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PeriodRevenueNet IncomeEPS
Q4 2025$17.2M$-53.2M$-0.30
FY 2025$42.7M$-204.4M$-1.21
Q3 2025$7.6M$-53.9M$-0.32
Q2 2025$8.7M$-50.5M$-0.31

Analyst Ratings

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B of A SecuritiesBuy
2026-03-27
Wells FargoOverweight
2026-03-27
MizuhoOutperform
2026-03-25
Canaccord GenuityBuy
2026-03-10
WedbushOutperform
2026-03-06

Trading Activity

Insider Trades

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RA CAPITAL MANAGEMENT, L.P.director, 10 percent owner:
BuyMon Mar 30
RA CAPITAL MANAGEMENT, L.P.director, 10 percent owner:
BuyMon Mar 30
RA CAPITAL MANAGEMENT, L.P.director, 10 percent owner:
BuyMon Mar 30
RA CAPITAL MANAGEMENT, L.P.director, 10 percent owner:
BuyMon Mar 30
TAKANASHI KENdirector
SellThu Mar 26

Company Info

Sector

Healthcare

Industry

Country

SG

Exchange

NASDAQ

Beta

-1.32

Wave Life Sciences Ltd., a clinical stage genetic medicine company, designs, optimizes, and produces novel stereopure oligonucleotides through PRISM, a discovery and drug developing platform. It is developing oligonucleotides target ribonucleic acid to reduce the expression of disease-promoting proteins or restore the production of functional proteins, or modulate protein expression. The company also develops WVE-004, a C9orf72 molecule for the treatment of amyotrophic lateral sclerosis and frontotemporal dementia; WVE-003, a mutant huntingtin SNP3 molecule for the treatment of Huntington's disease; WVE-N531, an Exon 53 molecule for the treatment of Duchenne muscular dystrophy; and ATXN3, a discovery stage program for the treatment of spinocerebellar ataxia 3, as well as multiple preclinical programs for CNS disorders. In addition, it focuses on developing GalNAc-conjugated AIMers to treat hepatic indications comprising Alpha-1 antitrypsin deficiency (AATD); and two preclinical programs, such as Usher syndrome type 2A (USH2A) and retinitis pigmentosa due to a P23H mutation in the RHO gene (RhoP23H) for the treatment of retinal diseases. It has collaboration agreements with Pfizer Inc., Takeda Pharmaceutical Company Limited, University of Oxford, University of Massachusetts, Western Washington University, Grenoble Institute of Neurosciences, IRBM S.p.A, University of Louisville, and University College London. The company was incorporated in 2012 and is based in Singapore.

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