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Smart Investors Daily
PM

NASDAQ · PMVP

PMV Pharmaceuticals, Inc.

Healthcare · Biotechnology

$1.43

Up+$0.03 (+2.10%)

Updated Sep 18, 2026, 1:08 AM

SID Score

4.2/10

Composite research score

Smart Money

Institutional and insider signal

Market cap
66.78M
P/E ratio
-0.81
Dividend yield
0.00%
52-week range
$1.04 – $1.73
Volume
1.02M
Avg. volume
564.7K

Price performance

PMVP price history

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Latest PMVP news

The latest Smart Investors Daily articles mentioning PMVP.

PMVP research

Overview

Company profile and research snapshot.

Company profile

PMV Pharmaceuticals Inc is a precision oncology company. The company is engaged in the research and development of small molecule, tumor-agnostic therapies targeting p53 mutations, which can eliminate cancer cells. Its pipeline rezatapopt PYNNACLE, rezatapopt and azacitidine, rezatapopt (PC14586), and PMV-586-101.

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Analyst outlook

Consensus and target data currently published for this company.

Consensus
Average target
$18.00
Implied upside
Analysts
PMVP recent ratings
DateFirmRatingTarget
Sep 4, 2026HC Wainwright & Co.Buy
May 13, 2026OppenheimerOutperform
Mar 20, 2025HC Wainwright & Co.Buy
Aug 20, 2024HC Wainwright & Co.Buy
May 30, 2024HC Wainwright & Co.Buy
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News briefing

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Yahoo · Sep 8, 2026

PMV Pharmaceuticals Appoints Philip Herman as Chief Commercial Officer

Commercial leadership appointment supports launch preparation for rezatapopt Company planning NDA submission for accelerated approval of rezatapopt in patients with platinum-resistant/refractory ovarian cancer in first quarter of 2027 PRINCETON, N.J., Sept. 08, 2026 (GLOBE NEWSWIRE) -- PMV Pharmaceuticals, Inc. (“PMV Pharma” or the “Company”; Nasdaq: PMVP), a precision oncology company pioneering the discovery and development of small molecule therapies targeting p53, today announced the appoint

Yahoo · Sep 1, 2026

PMV Pharma Raises $50.8 Million to Fuel Cancer Drug Push

PMV Pharmaceuticals Inc. (NASDAQ:PMVP) on Monday shared interim data from its Phase 2 PYNNACLE trial for rezatapopt, an investigational treatment for ovarian cancer.Based on this data, the company announced its plans to submit a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for accelerated approval of the drug.Efficacy HighlightsThe interim data, gathered up to May 14, 2026, focus on patients with platinum-resistant or refractory ovarian cancer bearing the TP53 Y220C

AI research layers

Interpretive context generated from the platform’s current data sources.

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