false000178527900017852792024-08-142024-08-14

 

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549

 

FORM 8-K

 

CURRENT REPORT

Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934

Date of Report (Date of earliest event reported): August 14, 2024

 

 

Metagenomi, Inc.

(Exact name of Registrant as Specified in Its Charter)

 

 

Delaware

001-41949

81-3909017

(State or Other Jurisdiction
of Incorporation)

(Commission File Number)

(IRS Employer
Identification No.)

 

 

 

 

 

5959 Horton Street

7th Floor

 

Emeryville, California

 

94608

(Address of Principal Executive Offices)

 

(Zip Code)

 

Registrant’s Telephone Number, Including Area Code: (510) 871-4880

 

Not Applicable

(Former Name or Former Address, if Changed Since Last Report)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Securities registered pursuant to Section 12(b) of the Act:


Title of each class

 

Trading
Symbol(s)

 


Name of each exchange on which registered

Common Stock, $0.0001 par value per share

 

MGX

 

Nasdaq Global Select Market

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).

Emerging growth company

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.

 


Item 2.02 Results of Operations and Financial Condition.

On August 14, 2024, Metagenomi, Inc. (the “Company”) announced its financial results for the quarter ended June 30, 2024 and additional business updates. A copy of the press release in connection with the announcement is being furnished as Exhibit 99.1 to this Current Report on Form 8-K.

The information in this Current Report on Form 8-K (including Exhibit 99.1 attached hereto) is intended to be furnished and shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended (the “Securities Act”), or the Exchange Act, except as expressly set forth by specific reference in such filing.

Item 9.01 Financial Statements and Exhibits.

(d) Exhibits

 

Exhibit No.

 

Description

99.1

 

Press Release Issued by Metagenomi, Inc. on August 14, 2024

104

 

Cover Page Interactive Data File (embedded within the Inline XBRL document)

 


SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

 

 

Metagenomi, Inc.

 

 

 

 

Date:

August 14, 2024

By:

/s/ Brian C. Thomas

 

 

 

Brian C. Thomas
Chief Executive Officer

 


Exhibit 99.1

img133734535_0.jpg 

 

Metagenomi Reports Business Updates and Second Quarter 2024 Financial Results

 

Declared development candidate MGX-001 for the treatment of hemophilia A;

plans to present 12-month NHP durability study data in September 2024

 

All Wave 1 Ionis collaboration programs advancing in lead optimization, unlocking potential for multiple development candidate nominations in 2025

 

Achieved milestone from partner Affini-T related to Metagenomi licensed technology

 

Well capitalized with $299.9M in cash, cash equivalents and available-for-sale marketable securities at the end of Q2 2024; cash runway anticipated to support operating plans into 2027

 

 

EMERYVILLE, Calif., August 14, 2024 -- Metagenomi, Inc. (Nasdaq: MGX) (Metagenomi), a precision genetic medicines company committed to developing curative therapeutics for patients using its proprietary, comprehensive metagenomics-derived gene editing toolbox, today provided a business update and reported second quarter 2024 financial results.

 

“We are progressing our pipeline while remaining laser focused on our vision to create curative genetic medicines by harnessing the power of our AI-driven metagenomics platform,” said Brian C. Thomas, PhD, CEO and Founder. “We have significantly advanced our wholly-owned program in hemophilia A, including recent positive regulatory interactions with Food and Drug Administration (FDA) and the declaration of MGX-001 as our lead development candidate. Our team has worked diligently to allow us to accelerate the data release from our 12-month nonhuman primate (NHP) durability study from the end of 2024 into September 2024. This study is an important step towards advancing MGX-001 as a potentially life-long curative treatment for both adults and children with hemophilia A, and demonstrating our ability to potentially achieve large targeted gene integration in patients using our metagenomics toolbox.”

 

Dr. Thomas continued, “We are also progressing our partnered programs and advancing our metagenomics-based toolbox. The foundation of our Ionis collaboration was strengthened by the addition of two high-value targets associated with cardiometabolic disease, and all collaboration programs have progressed into the lead optimization phase of development. We achieved a development milestone with Affini-T, where our team provided support for Affini-T’s regulatory filing related to Metagenomi licensed technology and current good manufacturing practices (cGMP) material supply. We continue to advance a broad range of technologies to support our goal of being able to address any disease by enabling any therapeutic genome edit in the human genome. Going forward, we remain well capitalized to execute our strategic priorities, with a cash runway into 2027.”

 

 

Second Quarter 2024 Business Updates and Key 2024-2025 Anticipated Milestones

 

Therapeutic Pipeline Updates

 

Metagenomi continues to advance its wholly-owned lead program in hemophilia A, designed as a one-time curative treatment for both adults and children.

 

 


 

o
The company engaged with FDA in the second quarter to discuss key aspects of the planned Investigational New Drug (IND) submission.
o
The company declared a lead development candidate (DC), MGX-001, meeting previously announced guidance for the timing of a DC nomination.
o
The company plans to accelerate the release of data from the 12-month NHP durability study for the lead hemophilia A program from late 2024 into September 2024. The 12-month NHP durability study was designed to show therapeutically relevant, durable expression of Factor VIII in NHPs, addressing a key concern which has impacted other genetic medicines programs in hemophilia A that have experienced loss of Factor VIII expression over time.
o
The company plans to initiate cGMP manufacturing and related IND enabling activities in 2024 and continue IND enabling activities in 2025.
o
As previously disclosed, the company remains on track to file an IND in hemophilia A in 2026.

 

Building on the recent success of the hemophilia A program, Metagenomi plans to advance additional wholly-owned therapeutic candidates targeting secreted protein disorders, leveraging the MGX-001 editing system with the goal of achieving targeted and durable gene expression.

 

o
This editing system consists of two components: a highly efficient and specific nuclease creates a precise cut at the albumin safe harbor gene locus after delivery by LNP; and an AAV vector delivered FVIII DNA template is inserted into the nuclease cut site by a naturally occurring DNA repair process.

 

Following selection of the remaining Wave 1 targets in the Ionis collaboration in the first quarter of 2024, all four therapeutic programs successfully advanced into the lead optimization phase in the second quarter of 2024.

 

o
All four therapeutic targets in Wave 1 collaboration focus on cardiometabolic diseases; the company announced Refractory Hypertension as the initial disease target leveraging the angiotensinogen pathway.
o
The company aims to demonstrate in vivo proof-of-concept in 2024, and advance NHP studies supporting DC nominations thereafter.
o
The company plans to nominate one to two DCs for cardiometabolic programs in 2025.

 

The company achieved a milestone in connection with its Affini-T collaboration, establishing cGMP gene editing reagents for cell therapy and filing related Drug Master Files with FDA to support an IND for Affini-T’s T-cell receptor-based therapy.

 

o
Metagenomi received 933,650 shares of Affini-T common stock upon achievement of this regulatory milestone.

 

Technology Platform Updates

 

Metagenomi achieved in vitro proof-of-concept for an undisclosed neuromuscular target with its ultra small editing system, a key milestone, opening up therapeutic potential for extrahepatic disease targets.
Metagenomi achieved in vitro proof-of-concept using its RNA-mediated integration system (RIGS) for undisclosed liver targets.
Metagenomi achieved multiplex base editing proof-of-concept and plans to present this data at a scientific conference in the second half of 2024.
Metagenomi achieved in vitro proof-of-concept in human cells for large gene integration using its potentially industry leading, compact CRISPR-associated transposase (CAST) technology, with a publication planned.
As previously disclosed, the company remains on track to demonstrate in vivo proof-of-concept for a large gene integration in 2026.

 

 

 


 

 

Other Business Updates

 

The company continues to exercise fiscal responsibility in prioritizing certain internal development programs while looking for collaboration partners to leverage other development opportunities.

 

o
Metagenomi is looking for a partner or licensee for further development of its program for primary hyperoxaluria type 1 (PH1). Previously disclosed data demonstrated preclinical proof-of-concept in an accepted disease model of PH1.
o
The company is continuing to focus its internal efforts on in vivo gene editing therapeutic approaches and pursue technology out-licensing for ex vivo cell therapy, where next generation gene editing systems are an important enabler of novel therapies.
o
Going forward, the company is not pursuing amyotrophic lateral sclerosis (ALS) based upon recent peer company clinical data regarding the lack of efficacy of Ataxin-2 as a therapeutic target for ALS.
o
The company is revising its pipeline design to consolidate earlier stage programs and make it easier to identify our near term pipeline priorities focused on in vivo gene editing and liver indications.

 

As a result of the acceleration of all four Wave 1 Ionis targets into lead optimization, as well as the company’s decision to deprioritize PH1, Metagenomi is revising to provide pipeline guidance only through year-end 2025, including the next one to two DC nominations in 2025. The company is maintaining its guidance for the planned IND filing for hemophilia A in 2026. The updated milestones are available in the corporate presentation on the company website.

 

 

Upcoming Events

 

Metagenomi plans to participate in the following events during the third quarter of 2024:

 

Wells Fargo Healthcare Conference, September 4-6, 2024, Everett, Massachusetts
H.C. Wainwright 26th Annual Global Investment Conference, September 9-11, 2024, New York City
Chardan 8th Annual Genetics Medicines Conference, September 30-October 1, 2024, New York City

 

Second Quarter 2024 Financial Results

 

Cash Position: Cash, cash equivalents, and available-for-sale marketable securities were $299.9 million as of June 30, 2024.
R&D Expenses: Research and development (R&D) expenses were $28.3 million for the three months ended June 30, 2024, compared to $22.7 million for the three months ended June 30, 2023.
G&A Expenses: General and administrative (G&A) expenses were $8.6 million for the three months ended June 30, 2024, compared to $6.6 million for the three months ended June 30, 2023.

 

 

About Metagenomi

 

Metagenomi is a precision genetic medicines company committed to developing curative therapeutics for patients using its proprietary, comprehensive metagenomics-derived toolbox. Metagenomi is harnessing the power of metagenomics, the study of genetic material recovered from the natural environment, to unlock four billion years of microbial evolution to discover and develop a suite of novel editing tools capable of correcting any type of genetic mutation found

 

 


 

anywhere in the genome. Its comprehensive genome editing toolbox includes programmable nucleases, base editors, and RNA and DNA-mediated integration systems (including prime editing systems and clustered regularly interspaced short palindromic repeat associated transposases). Metagenomi believes its diverse and modular toolbox positions the company to access the entire genome and select the optimal tool to unlock the full potential of genome editing for patients. For more information, please visit https://​metageno​mi​.co.

 

Cautionary Note Regarding Forward-Looking Statements

 

This press release contains “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934, each as amended. Such statements, which are often indicated by terms such as ​“anticipate,” “believe,” “could,” “estimate,” “expect,” “goal,” “intend,”​ “look forward to,” “may,” “plan,” “potential,” “predict,”​ “project,”​ “should,” “will,” “would” and similar expressions, include, but are not limited to, any statements relating to our growth strategy and product development programs, including the timing of and our ability to conduct IND-enabling studies, make regulatory filings such as INDs, statements concerning the potential of therapies and product candidates, statements concerning the timing of data presentations and publications, and any other statements that are not historical facts. Forward looking statements are based on management’s current expectations and are subject to risks and uncertainties that could negatively affect our business, operating results, financial condition, and stock value. Factors that could cause actual results to differ materially from those currently anticipated include: risks relating to our growth strategy; our ability to obtain, perform under, and maintain financing and strategic agreements and relationships; risks relating to the results of research and development activities; risks relating to the timing of starting and completing clinical trials; uncertainties relating to preclinical and clinical testing; our dependence on third party suppliers; our ability to attract, integrate and retain key personnel; the early stage of products under development; our need for substantial additional funds; government regulation; patent and intellectual property matters; competition; as well as other risks described in ​“Risk Factors,” in our most recent Form 10-K and our most recent 10-Qs on file with the Securities and Exchange Commission. We expressly disclaim any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in our expectations or any changes in events, conditions or circumstances on which any such statement is based, except as required by law, and we claim the protection of the safe harbor for forward-looking statements contained in the Private Securities Litigation Reform Act of 1995.

 

Investor Contact:

Simon Harnest - CIO, SVP Investor Relations

simon@​metagenomi.​co

 

Media Contact:

Ashlye Hodge - Communications Manager

ashlye@​metagenomi.​co

 

 


 

Condensed Financial Statements

 

Condensed Consolidated Balance Sheet Data

(Unaudited)

 

 

June 30,

 

 

December 31,

 

(in thousands)

 

2024

 

 

2023

 

Cash, cash equivalents and available-for-sale marketable securities

 

$

299,921

 

 

$

271,182

 

Total assets

 

$

385,905

 

 

$

364,842

 

Total liabilities

 

$

116,486

 

 

$

149,668

 

Redeemable convertible preferred stock

 

$

 

 

$

350,758

 

Total stockholders’ equity (deficit)

 

$

269,419

 

 

$

(135,584

)

Total liabilities, redeemable convertible preferred stock and stockholders’ equity (deficit)

 

$

385,905

 

 

$

364,842

 

 

 

Condensed Consolidated Statements of Operations

(Unaudited)

 

 

Three Months Ended
June 30,

 

 

Six Months Ended
June 30,

 

(In thousands, except share and per share data)

 

2024

 

 

2023

 

 

2024

 

 

2023

 

Collaboration revenue

 

$

20,008

 

 

$

11,337

 

 

$

31,167

 

 

$

19,994

 

Operating expenses:

 

 

 

 

 

 

 

 

 

 

 

 

Research and development

 

 

28,320

 

 

 

22,681

 

 

 

59,759

 

 

 

42,811

 

General and administrative

 

 

8,551

 

 

 

6,619

 

 

 

17,303

 

 

 

13,084

 

Total operating expenses

 

 

36,871

 

 

 

29,300

 

 

 

77,062

 

 

 

55,895

 

Loss from operations

 

 

(16,863

)

 

 

(17,963

)

 

 

(45,895

)

 

 

(35,901

)

Other income (expense):

 

 

 

 

 

 

 

 

 

 

 

 

Interest income

 

 

3,976

 

 

 

3,967

 

 

 

7,910

 

 

 

7,970

 

Change in fair value of long-term investments

 

 

 

 

 

2,870

 

 

 

 

 

 

2,870

 

Other income (expense), net

 

 

(51

)

 

 

16

 

 

 

(101

)

 

 

15

 

Total other income, net

 

 

3,925

 

 

 

6,853

 

 

 

7,809

 

 

 

10,855

 

Net loss before benefit (provision) for income taxes

 

 

(12,938

)

 

 

(11,110

)

 

 

(38,086

)

 

 

(25,046

)

Benefit (provision) for income taxes

 

 

2,199

 

 

 

(1,898

)

 

 

2,199

 

 

 

(4,095

)

Net loss

 

$

(10,739

)

 

$

(13,008

)

 

$

(35,887

)

 

$

(29,141

)

Net loss per share attributable to common stockholders, basic and diluted

 

$

(0.29

)

 

$

(3.82

)

 

$

(1.24

)

 

$

(8.56

)

Weighted average common shares outstanding, basic and diluted

 

 

36,625,291

 

 

 

3,404,585

 

 

 

28,901,399

 

 

 

3,404,585

 

 

 

 

 

 


 

 

 

 

 

 

 

 


v3.24.2.u1
Document And Entity Information
Aug. 14, 2024
Cover [Abstract]  
Document Type 8-K
Amendment Flag false
Document Period End Date Aug. 14, 2024
Entity Registrant Name Metagenomi, Inc.
Entity Central Index Key 0001785279
Entity Emerging Growth Company true
Entity File Number 001-41949
Entity Incorporation, State or Country Code DE
Entity Tax Identification Number 81-3909017
Entity Address, Address Line One 5959 Horton Street
Entity Address, Address Line Two 7th Floor
Entity Address, City or Town Emeryville
Entity Address, State or Province CA
Entity Address, Postal Zip Code 94608
City Area Code (510)
Local Phone Number 871-4880
Entity Information, Former Legal or Registered Name Not Applicable
Written Communications false
Soliciting Material false
Pre-commencement Tender Offer false
Pre-commencement Issuer Tender Offer false
Entity Ex Transition Period true
Title of 12(b) Security Common Stock, $0.0001 par value per share
Trading Symbol MGX
Security Exchange Name NASDAQ

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