Compare · CEMI vs NTLA
CEMI vs NTLA
Side-by-side comparison of Chembio Diagnostics Inc. (CEMI) and Intellia Therapeutics Inc. (NTLA): market cap, price performance, sector, and recent activity on the wire.
Summary
- Both CEMI and NTLA operate in Biotechnology: In Vitro & In Vivo Diagnostic Substances (Health Care), so they compete in similar markets.
- NTLA is the larger of the two at $1.61B, about 64.4x CEMI ($25.0M).
- NTLA has hit the wire 3 times in the past 4 weeks while CEMI has been quiet.
- NTLA has more recent analyst coverage (25 ratings vs 1 for CEMI).
- Company
- Chembio Diagnostics Inc.
- Intellia Therapeutics Inc.
- Price
- $0.46+2.63%
- $16.00+0.82%
- Market cap
- $25.0M
- $1.61B
- 1M return
- -
- +2.71%
- 1Y return
- -
- +60.67%
- Industry
- Biotechnology: In Vitro & In Vivo Diagnostic Substances
- Biotechnology: In Vitro & In Vivo Diagnostic Substances
- Exchange
- NASDAQ
- NASDAQ
- IPO
- 2016
- News (4w)
- 0
- 3
- Recent ratings
- 1
- 25
Chembio Diagnostics Inc.
Chembio Diagnostics, Inc., together with its subsidiaries, develops, manufactures, and commercializes point-of-care (POC) diagnostic tests that are used to detect or diagnose diseases. The company offers tests for COVID-19, HIV and Syphilis, and Zika virus. It also develops tests for malaria, dengue, Hepatitis C, chikungunya, Chagas, ebola, leishmaniasis, lassa, marburg, leptospirosis, Rickettsia, and Burkholderia diseases. The company sells its products under the STAT-PAK, SURE CHECK, STAT VIEW, and DPP trademarks, as well as under the private labels of its marketing partners to medical laboratories and hospitals, governmental and public health entities, non-governmental organizations, medical professionals, and retail establishments in the United States and internationally. It has collaboration agreements with Bill & Melinda Gates Foundation, The Paul G. Allen Family Foundation, The Oswaldo Cruz Foundation, and the Foundation for Innovative New Diagnostics, as well as U.S. government agencies, such as Centers for Disease Control and Prevention, the Biomedical Advanced Research and Development Authority of the U.S. Department of Health and Human Services, and the U.S. Department of Agriculture. Chembio Diagnostics, Inc. was founded in 1985 and is headquartered in Hauppauge, New York.
Intellia Therapeutics Inc.
Intellia Therapeutics, Inc., a genome editing company, focuses on the development of therapeutics. It utilizes a biological tool known as the Clustered, Regularly Interspaced Short Palindromic Repeats/CRISPR associated 9 (CRISPR/Cas9) system. The company's in vivo programs include NTLA-2001, which is in Phase 1 clinical trial for the treatment of transthyretin amyloidosis; and NTLA-2002 for the treatment of hereditary angioedema, as well as other liver-focused programs comprising hemophilia A and hemophilia B, hyperoxaluria Type 1, and alpha-1 antitrypsin deficiency. Its ex vivo pipeline includes NTLA-5001 for the treatment of acute myeloid leukemia; and proprietary programs focused on developing engineered cell therapies to treat various oncological and autoimmune disorders. Intellia Therapeutics, Inc. has license and collaboration agreements with Novartis Institutes for BioMedical Research, Inc. to engineer hematopoietic stem cells for the treatment of sickle cell disease; Regeneron Pharmaceuticals, Inc. to co-develop potential products for the treatment of hemophilia A and hemophilia B; and Ospedale San Raffaele. The company was formerly known as AZRN, Inc. and changed its name to Intellia Therapeutics, Inc. in July 2014. Intellia Therapeutics, Inc. was incorporated in 2014 and is headquartered in Cambridge, Massachusetts.
Latest CEMI
- SEC Form 15-12G filed by Chembio Diagnostics Inc.
- SEC Form SC 13D/A filed by Chembio Diagnostics Inc. (Amendment)
- SEC Form EFFECT filed by Chembio Diagnostics Inc.
- SEC Form EFFECT filed by Chembio Diagnostics Inc.
- SEC Form EFFECT filed by Chembio Diagnostics Inc.
- SEC Form EFFECT filed by Chembio Diagnostics Inc.
- SEC Form EFFECT filed by Chembio Diagnostics Inc.
- SEC Form 4 filed by Angelico Paul
- SEC Form 4 filed by Acheson David
- SEC Form 4 filed by Eberly Richard
Latest NTLA
- Intellia Therapeutics to Report Topline Data from Global Phase 3 HAELO Clinical Trial of Lonvoguran Ziclumeran in Hereditary Angioedema on April 27, 2026
- SEC Form 8-K filed by Intellia Therapeutics Inc.
- The Credibility Filter Wall Street Uses to Sort Biotech Winners
- Intellia Therapeutics Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
- Amendment: SEC Form SCHEDULE 13G/A filed by Intellia Therapeutics Inc.
- Intellia Therapeutics Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
- EVP, General Counsel Basta James was granted 46,080 shares and sold $16,688 worth of shares (1,211 units at $13.78), increasing direct ownership by 40% to 156,794 units (SEC Form 4)
- President and CEO Leonard John M was granted 156,400 shares, increasing direct ownership by 15% to 1,169,739 units (SEC Form 4)
- VP, Chief Accounting Officer Dube Michael P was granted 17,250 shares, increasing direct ownership by 33% to 69,527 units (SEC Form 4)
- EVP, Chief Financial Officer Dulac Edward J Iii was granted 61,280 shares, increasing direct ownership by 61% to 160,963 units (SEC Form 4)