Mammoth Biosciences

Mammoth Biosciences

CRISPR-based diagnostic platform developer

Overview

Mammoth Biosciences uses CRISPR technology to create rapid molecular diagnostic tests that can identify diseases, including COVID-19, at or near the point of care. Its CRISPR-based platform detects genetic material from pathogens, enabling quick, on-site results that patients can discuss with healthcare providers without sending samples to distant labs. The company earns revenue through partnerships (such as with GSK Consumer Healthcare) and the sale of its diagnostic products and services to healthcare providers and research institutions. By collaborating with scientists and institutions, Mammoth aims to expand the range of conditions its platform can detect and to improve the speed and accessibility of diagnostic testing. In short, Mammoth Biosciences focuses on practical, fast, and accessible molecular diagnostics built on CRISPR technology, targeting healthcare and research markets with a goal of broadening rapid testing options globally.

About Mammoth Biosciences

Simplify's Rating
Why Mammoth Biosciences is rated
C-
Rated C on Competitive Edge
Rated C on Growth Potential
Rated D+ on Differentiation

Industries

Biotechnology

Healthcare

Company Size

51-200

Company Stage

Late Stage VC

Total Funding

$363.2M

Headquarters

Brisbane, California

Founded

2017

People at Mammoth Biosciences

People at Mammoth Biosciences who can refer or advise you

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Simplify's Take

What believers are saying

  • Abu Dhabi partnership enables MB-111 clinical trials and local GMP lipid nanoparticle manufacturing starting June 25, 2026.
  • VedaBio licensing expands Mammoth’s commercial reach in molecular diagnostics beyond therapeutics through nonexclusive CRISPR tech use.
  • Ultracompact systems support base, reverse transcriptase, and epigenetic editing modalities enabling therapies beyond liver targeting.

What critics are saying

  • Intense competition from Editas Medicine’s EDIT-101 with 45–60% liver editing efficiency could stall MB-111 in 12–18 months.
  • Transient liver function elevations in primates risk FDA clinical hold within 6–12 months with high impact on development.
  • Intellia Therapeutics IP lawsuit over ultracompact nuclease claims could invalidate core patents within 12–24 months, causing existential loss.

What makes Mammoth Biosciences unique

  • Mammoth uses ultracompact CasPhi CRISPR systems for in vivo editing in hard-to-reach tissues beyond the liver.
  • Co-founded by Nobel laureate Jennifer Doudna, Mammoth holds exclusive rights to Cas12, Cas13, and Cas14 for diagnostics.
  • MB-111 is a first-in-class, single-dose therapy targeting APOC3 with sustained liver editing in nonhuman primates.

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Funding

Total Funding

$363.2M

Above

Industry Average

Funded Over

7 Rounds

Notable Investors:
Late VC funding comparison data is currently unavailable. We're working to provide this information soon!
Late VC Funding Comparison
Coming Soon

Benefits

Medical, dental, & vision

401(k)

Unlimited vacation

Transportation subsidy

Onsite amenities

Happy hours

Growth & Insights and Company News

Headcount

6 month growth

-1%

1 year growth

0%

2 year growth

1%
Dubai Standard
Jun 25th, 2026
Abu Dhabi partners with a US biotechnology company to develop advanced gene-editing therapies.

Abu Dhabi partners with a US biotechnology company to develop advanced gene-editing therapies. June 25, 2026 The new collaboration seeks to advance the development of treatments for rare and inherited diseases. Abu Dhabi has taken another significant step in advancing precision medicine after the Department of Health - Abu Dhabi (DoH), M42, and US-based Mammoth Biosciences signed a memorandum of understanding (MoU) to develop gene-editing therapies for rare and inherited diseases. The agreement was announced at the BIO International Convention 2026 in San Diego and is aimed at strengthening Abu Dhabi's growing life sciences sector by supporting clinical research, advanced therapy manufacturing, and scientific innovation. Officials said the collaboration builds on the emirate's ongoing investments in genomics and precision medicine, with the goal of translating genetic research into treatments that can benefit patients in the UAE and globally. The partnership will leverage insights from the Emirati Genome Programme to support the development of next-generation therapies for inherited diseases, while also expanding research and manufacturing capabilities in Abu Dhabi. Driving the future of precision medicine. Dr Noura Al Ghaithi, Undersecretary of the Department of Health - Abu Dhabi, said the partnership reflects the emirate's long-term commitment to advancing healthcare innovation. "Abu Dhabi has built a strong foundation in genomics and precision medicine through sustained investments in research and innovation. The next step is translating these insights into therapies that can address some of the most complex diseases affecting communities in our region and globally," she said. Under the agreement, the Department of Health - Abu Dhabi will provide the regulatory and research framework, while M42 will contribute its genomics expertise, healthcare network, and clinical research infrastructure. Mammoth Biosciences will bring its CRISPR-based gene-editing technology to the collaboration. Dr Fahed Al Marzooqi, Chief Executive Officer of Integrated Health Solutions at M42, said the Emirati Genome Programme has generated valuable insights into the health needs of the local population. "Through this collaboration, we are building on that foundation by supporting the development of advanced therapies while strengthening Abu Dhabi's research, clinical, and manufacturing capabilities," he said. Building local expertise and manufacturing capacity. Mammoth Biosciences, co-founded by Nobel Prize-winning scientist Jennifer Doudna, develops gene-editing technologies aimed at treating inherited diseases by correcting genetic mutations rather than merely managing symptoms. The agreement also includes plans to introduce Mammoth's lead clinical candidate, MB-111, into Abu Dhabi's clinical research ecosystem and support advanced gene-therapy trials in the emirate. It also outlines plans to develop advanced therapy manufacturing capabilities, starting with lipid nanoparticle production and later expanding into fully integrated manufacturing facilities. In addition, the partnership will support training programmes designed to build local expertise in CRISPR-based gene-editing technologies and strengthen the UAE's specialised healthcare workforce. The collaboration aligns with Abu Dhabi's Health, Endurance, Longevity and Medicine (HELM) Cluster, which aims to accelerate healthcare innovation by integrating research, clinical development, manufacturing, and commercialisation within a unified ecosystem. Officials said the agreement represents another milestone in Abu Dhabi's efforts to establish itself as a global hub for life sciences, advanced therapies, and precision medicine.

HealthTech HotSpot
Jan 9th, 2026
Mammoth Biosciences to Present at 44th Annual J.P. Morgan Healthcare Conference

Mammoth Biosciences to present at 44th Annual J.P. Morgan Healthcare Conference. BRISBANE, Calif. - (BUSINESS WIRE) - #CRISPR - Mammoth Biosciences, Inc., a biotechnology company harnessing its proprietary next-generation in vivo CRISPR gene editing platform to create potential one-time curative therapies, today announced its participation in the upcoming 44th Annual J.P. Morgan Healthcare Conference. Trevor Martin, Ph.D., co-founder and CEO, will provide a corporate overview with key business updates related to Mammoth Biosciences' pipeline and platform on Thursday, January 15 at 7.30 am PT in San Francisco. About Mammoth Biosciences Mammoth Biosciences is a biotechnology company focused on leveraging its proprietary ultracompact CRISPR systems to develop potential long-term curative therapies for patients with life-threatening and debilitating diseases. Founded by CRISPR pioneer and Nobel laureate Jennifer Doudna and Trevor Martin, Janice Chen, and Lucas Harrington, the company's ultracompact systems are designed to be more specific and packageable to enable in vivo gene editing in difficult to reach tissues utilizing both nuclease applications and new editing modalities beyond double stranded breaks, including base editing, reverse transcriptase editing, and epigenetic editing. The company is building out its wholly owned pipeline of potential in vivo gene editing therapeutics and capabilities and has partnerships with leading pharmaceutical and biotechnology companies to broaden the reach of its innovative and proprietary technology platform. Mammoth Biosciences' deep science and industry experience, along with a robust and differentiated intellectual property portfolio, have enabled the company to further its mission to transform the lives of patients and deliver on the promise of CRISPR technologies. For more information, please visit www.mammoth.bio or follow Mammoth on LinkedIn or X. Media Contact: Mohana Ray Email: [email protected] Phone: 312-506-5210

CRISPR Medicine News
Oct 1st, 2025
Mammoth Biosciences to Present Preclinical Data on MB-111 at the European Society of Gene & Cell Therapy 32nd Annual Congress

Mammoth Biosciences to present preclinical data on MB-111 at the European Society of Gene & Cell Therapy 32nd Annual Congress.

360Dx
Sep 9th, 2025
VedaBio Licenses Mammoth Biosciences Diagnostic CRISPR Technology

NEW YORK - VedaBio has entered into a nonexclusive licensing agreement with Mammoth Biosciences for the use of certain Mammoth CRISPR-based technologies for diagnostic applications, the firms announced on Tuesday.

Labiotech.eu
Oct 10th, 2024
12 Biotech Unicorns Revolutionizing The Future Of Healthcare

Have you ever heard of a biotech unicorn? Although a mythological creature might be what first springs to mind, a unicorn in the business world actually refers to a privately owned company valued at more than $1 billion. Some world-renowned former unicorns include Airbnb, Facebook, and Google. The reason they are called “unicorns” is because it is traditionally very rare for a company to achieve this valuation.In the biotech world, there are only a select few companies with unicorn status that are working on therapeutics. In this article, we take a closer look at 12 biotech unicorns rated in order of their valuations according to CB Insights.Table of contentsAbogen BiosciencesAbogen Biosciences is a Chinese biotech company and is valued at $3.7 billion. This comes as no surprise after it raised $700 million in series C funding back in August 2021, marking one of the largest private biotech funding rounds ever and obliterating the fundraising record for a Chinese mRNA vaccine developer. It then followed this round with another impressive series C+ round in November of the same year, in which it raised $300 million.Abogen is part of a rare breed of Chinese biotechs, having actually developed all of its key messenger RNA (mRNA) platform technologies itself, across mRNA synthesis, delivery, and manufacturing

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