MARKET

RLAY

RLAY

Relay Therapeutics, Inc.
NASDAQ
6.16
-0.20
-3.07%
After Hours: 6.26 +0.11 +1.71% 18:44 04/25 EDT
OPEN
6.16
PREV CLOSE
6.35
HIGH
6.21
LOW
5.82
VOLUME
1.39M
TURNOVER
0
52 WEEK HIGH
13.32
52 WEEK LOW
5.70
MARKET CAP
814.52M
P/E (TTM)
-2.2062
1D
5D
1M
3M
1Y
5Y
Weekly Report: what happened at RLAY last week (0415-0419)?
Weekly Report · 4d ago
Weekly Report: what happened at RLAY last week (0408-0412)?
Weekly Report · 04/15 10:08
Relay Therapeutics to Participate in Upcoming Investor Conferences
Barchart · 04/11 15:05
FATE, ALPN and RLAY are among after hour movers
On the Move FATE, ALPN and RLAY are among after hour movers. Rallybio Corporation and Alpine Immune Sciences are among the biggest gainers. Performant Financial and NioCorp Developments are the biggest losers in the after hour.
Seeking Alpha · 04/10 21:20
12 Health Care Stocks Moving In Wednesday's After-Market Session
Rallybio shares rose 31.9% to $2.15 during Wednesday's after-market session. The company's market cap stands at $81.2 million. Vera Therapeutics (NASDAQ:VERA) shares increased by 10.52% during the session.
Benzinga · 04/10 20:31
Weekly Report: what happened at RLAY last week (0401-0405)?
Weekly Report · 04/08 10:11
Weekly Report: what happened at RLAY last week (0325-0329)?
Weekly Report · 04/01 10:10
Weekly Report: what happened at RLAY last week (0318-0322)?
Weekly Report · 03/25 10:12
More
About RLAY
Relay Therapeutics Inc. is a clinical-stage precision medicine company. The Company is focused on enhancing small molecule therapeutic discovery in targeted oncology and genetic disease indications. The Company’s Dynamo platform integrates an array of computational and experimental approaches designed to drug protein targets that have previously been intractable or inadequately addressed. The Company’s lead product candidates, such as RLY-2608, Lirafugratinib (RLY-4008), and Migoprotafib (GDC-1971). RLY-2608 is an allosteric, pan-mutant and isoform-selective phosphoinostide 3 kinase alphas (PI3Kα), inhibitor. RLY-4008, is a potent, selective, and oral small molecule inhibitor of FGFR2, a receptor tyrosine kinase that is frequently altered in certain cancers. GDC-1971 is an inhibitor of Src homology region 2 domain-containing phosphatase-2 (SHP2), as a monotherapy in patients with advanced or metastatic solid tumors.

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