MYRIAD GENETICS INC

NASDAQ: MYGN (Myriad Genetics, Inc.)

Kemas kini terakhir: 05 Dec, 5:08PM

16.36

-0.24 (-1.45%)

Penutupan Terdahulu 16.60
Buka 16.50
Jumlah Dagangan 507,737
Purata Dagangan (3B) 793,034
Modal Pasaran 1,489,335,936
Harga / Pendapatan (P/E Ke hadapan) 140.85
Harga / Jualan (P/S) 1.43
Harga / Buku (P/B) 1.64
Julat 52 Minggu
14.72 (-10%) — 29.30 (79%)
Tarikh Pendapatan 25 Feb 2025 - 3 Mar 2025
Margin Keuntungan -14.09%
Margin Operasi (TTM) -8.35%
EPS Cair (TTM) -1.28
Pertumbuhan Hasil Suku Tahunan (YOY) 11.20%
Jumlah Hutang/Ekuiti (D/E MRQ) 19.56%
Nisbah Semasa (MRQ) 1.90
Aliran Tunai Operasi (OCF TTM) -70.00 M
Aliran Tunai Bebas Leveraj (LFCF TTM) -52.90 M
Pulangan Atas Aset (ROA TTM) -5.35%
Pulangan Atas Ekuiti (ROE TTM) -16.40%

Arah Aliran Pasaran

Jangka Pendek Jangka Sederhana
Industri Diagnostics & Research (US) Bercampur Bercampur
Diagnostics & Research (Global) Bercampur Bercampur
Stok Myriad Genetics, Inc. Menurun Menurun

AISkor Stockmoo

-0.6
Konsensus Penganalisis -1.5
Aktiviti Orang Dalam -3.0
Volatiliti Harga 0.5
Purata Bergerak Teknikal 1.5
Osilator Teknikal -0.5
Purata -0.60

Saham Serupa

Stok Modal Pasaran DY P/E (TTM) P/B
MYGN 1 B - - 1.64
MEDP 10 B - 29.56 12.42
RDNT 5 B - 402.94 6.53
GH 4 B - - 55.67
VCYT 3 B - - 2.69
NEO 2 B - - 2.32

Myriad Genetics is a molecular diagnostics company that provides testing services designed to assess an individual’s risk of developing a disease. The firm produces MyRisk, a 48-gene panel with the capability to identify the elevated risk of developing 11 types of cancer. Other diagnostic products include BRACAnalysis CDx, the FDA-approved companion diagnostic for PARP inhibitors; GeneSight, which helps improve responses to psychotropic drugs for patients suffering from depression; and Prequel, a noninvasive prenatal test. Precise Oncology Solutions, launched in 2022, combines Precise Tumor with companion diagnostic and prognostic tests such as MyChoice CDx, Prolaris, and EndoPredict. The firm offers biomarker discovery and companion diagnostic services to pharma and biotech companies.

Sektor Healthcare
Industri Diagnostics & Research
Gaya Pelaburan Small Growth
% Dimiliki oleh Orang Dalam 2.01%
% Dimiliki oleh Institusi 102.30%
Julat 52 Minggu
14.72 (-10%) — 29.30 (79%)
Julat Harga Sasaran
13.00 (-20%) — 24.00 (46%)
Tinggi 24.00 (Piper Sandler, 46.70%) Pegang
Median 21.00 (28.36%)
Rendah 13.00 (B of A Securities, -20.54%) Jual
Purata 19.40 (18.58%)
Jumlah 4 Pegang, 1 Jual
Harga Purata @ Panggilan 15.44
Syarikat Tarikh Harga Sasaran Panggilan Harga @ Panggilan
B of A Securities 13 Dec 2024 13.00 (-20.54%) Jual 14.43
UBS 10 Dec 2024 18.00 (10.02%) Pegang 15.34
Leerink Partners 09 Dec 2024 21.00 (28.36%) Pegang 14.88
Morgan Stanley 18 Nov 2024 21.00 (28.36%) Pegang 15.22
Piper Sandler 11 Nov 2024 24.00 (46.70%) Pegang 17.31
Nama Purata Belian ($) Purata Jualan ($) Jumlah Net Jumlah Nilai Bersih ($)
DAVIS MARK STEVEN 15.34 - 22,816 349,997
RAHA SAMRAAT S. - 14.51 -29,578 -429,177
Jumlah Keseluruhan Kuantiti Bersih -6,762
Jumlah Keseluruhan Nilai Bersih ($) -79,179
Purata Pembelian Keseluruhan ($) 15.34
Purata Jualan Keseluruhan ($) 14.51
Nama Pemegang Tarikh Jenis Kuantiti Harga Nilai ($)
RAHA SAMRAAT S. Pegawai 11 Dec 2024 Dibuang (-) 29,578 14.51 429,177
DAVIS MARK STEVEN Pengarah 10 Dec 2024 Diperolehi (+) 22,816 15.34 349,997
Tarikh Jenis Butiran
19 Dec 2024 Pengumuman Myriad Genetics’ RiskScore Study Named One of the Top 10 Significant Advances in Genomic Medicine in American Journal of Human Genetics
10 Dec 2024 Pengumuman Myriad Genetics’ Portfolio Elevated by Updated NCCN Prostate Cancer Guidelines
10 Dec 2024 Pengumuman Myriad Genetics Provides Update on Discussions with UnitedHealthcare regarding Medical Policy for Pharmacogenetic Testing
10 Dec 2024 Pengumuman Myriad Genetics Expands Board of Directors with Election of Mark S. Davis as New Board Member
09 Dec 2024 Pengumuman NCCN Prostate Cancer Guidelines Reinforce Status of Myriad Genetics' Prolaris® Test as an 'Advanced Tool' Recommended for Prognostic Assessment
09 Dec 2024 Pengumuman Myriad Genetics to Present New Data at San Antonio Breast Cancer Symposium
20 Nov 2024 Pengumuman Myriad Genetics Announces Incorporation of its Proprietary HRD platform in Illumina’s Updated Comprehensive Gene Panel Assay, TruSight™ Oncology 500 v2
19 Nov 2024 Pengumuman Myriad Genetics Announces Prequel® Prenatal Screening Can Now be Performed Eight Weeks into Pregnancy
13 Nov 2024 Pengumuman Myriad Genetics Expands Access to At-Home Early Fetal Sex DNA Test with Retail Launch
07 Nov 2024 Pengumuman Myriad Genetics Reports Third Quarter 2024 Financial Results; Updates 2024 Financial Guidance
04 Nov 2024 Pengumuman Myriad Genetics Comments on UnitedHealthcare’s Updated Medical Policy for Pharmacogenetic Testing
30 Oct 2024 Pengumuman Myriad Genetics to Release Third Quarter 2024 Financial Results on November 7, 2024
16 Oct 2024 Pengumuman Myriad Genetics and jscreen™ Announce Strategic Partnership to Advance Health Equity and Genetic Testing Access
15 Oct 2024 Pengumuman Myriad Genetics and Flatiron Health Partner to Make Genetic Testing More Accessible with Electronic Medical Record Integration
08 Oct 2024 Pengumuman Myriad Genetics Announces Five Research Collaborations to Study the Use of MRD Testing in Breast Cancer
03 Oct 2024 Pengumuman Myriad Genetics and Ultima Genomics to Explore the UG 100™ Sequencing Platform to Advance Clinical Test Offerings in Oncology and Reproductive Genomics
01 Oct 2024 Pengumuman Myriad Genetics Announces Third Patent Granted for Molecular Residual Disease (MRD) with Early Priority Date
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