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Smart Investors Daily
OS

NASDAQ · OSA

ProSomnus, Inc.

Healthcare · Medical - Devices

$0.47

Up+$0.00 (+0.00%)

Updated Aug 24, 2026, 12:43 AM

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Market cap
8.18M
P/E ratio
-0.32
Dividend yield
0.00%
52-week range
— – —
Volume
58.85K
Avg. volume
58.85K

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OSA research

Overview

Company profile and research snapshot.

Company profile

ProSomnus, Inc. manufactures precision oral appliance therapy devices for the treatment of obstructive sleep apnea (OSA). The company was founded in 2016 and is based in Pleasanton, California.

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Analyst outlook

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Consensus
Average target
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Analysts
OSA recent ratings
DateFirmRatingTarget
Jan 22, 2024Alliance Global PartnersBuy
Nov 10, 2023Craig-HallumHold
Sep 26, 2023Roth MKMBuy
Apr 18, 2023Roth MKMBuy
Apr 3, 2023Craig-HallumBuy
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globenewswire.com · Dec 3, 2025

Incannex Granted FDA Fast Track Designation for IHL-42X in Obstructive Sleep Apnea (OSA)

MELBOURNE, Australia and NEW YORK, Dec. 03, 2025 (GLOBE NEWSWIRE) -- Incannex Healthcare Inc. (Nasdaq: IXHL), a clinical-stage biopharmaceutical company developing innovative combination therapies, announces that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation for IHL-42X, the Company's oral fixed-dose combination product candidate for the treatment of obstructive sleep apnea (OSA). The Fast Track designation was supported by promising safety, efficacy, and pharmacokinetic results from the three clinical trials completed to date within the IHL-42X development program.

globenewswire.com · Sep 30, 2025

Mineralys Therapeutics Completes Enrollment in Phase 2 EXPLORE-OSA Trial of Lorundrostat in Obstructive Sleep Apnea and Hypertension

~ Topline results from the EXPLORE-OSA trial are anticipated in 1Q 2026 ~ RADNOR, Pa., Sept. 30, 2025 (GLOBE NEWSWIRE) -- Mineralys Therapeutics, Inc. (Nasdaq: MLYS), a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease (CKD), obstructive sleep apnea (OSA) and other diseases driven by dysregulated aldosterone, today announced that it has completed enrollment in its Phase 2 EXPLORE-OSA trial of lorundrostat in participants with moderate-to-severe OSA and hypertension.

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