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Monogram Technologies Reports Third Quarter 2024 Financial Results

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Monogram Technologies (NASDAQ:MGRM) reported Q3 2024 financial results, highlighting an upsized and oversubscribed $13 million public offering. The company submitted a 510(k) premarket filing for its mBȏs TKA System and received an Additional Information Request from FDA. Key financials include R&D expenses of $2.2 million, marketing expenses of $1.8 million, and a net loss of $5.0 million. Cash position stood at $16.6 million as of September 30, 2024. The company secured a strategic collaboration with Shalby for multicenter clinical trials in India and was named Orthopedic Joint Replacement Company of the Year 2024.

Monogram Technologies (NASDAQ:MGRM) ha riportato i risultati finanziari del terzo trimestre 2024, evidenziando un aumento e un'eccedenza nell'offerta pubblica di 13 milioni di dollari. L'azienda ha presentato una richiesta di autorizzazione premarket 510(k) per il suo sistema mBȏs TKA e ha ricevuto una Richiesta di Informazioni Aggiuntive dalla FDA. I principali dati finanziari includono spese per R&S di 2,2 milioni di dollari, spese di marketing per 1,8 milioni di dollari e una perdita netta di 5,0 milioni di dollari. La posizione di cassa ammontava a 16,6 milioni di dollari al 30 settembre 2024. L'azienda ha assicurato una collaborazione strategica con Shalby per studi clinici multicentrici in India ed è stata nominata Azienda dell'Anno 2024 per la Sostituzione Articolare Ortopedica.

Monogram Technologies (NASDAQ:MGRM) informó los resultados financieros del tercer trimestre de 2024, destacando una oferta pública ampliada y sobree suscrita de 13 millones de dólares. La compañía presentó una solicitud de premercado 510(k) para su sistema mBȏs TKA y recibió una Solicitud de Información Adicional de la FDA. Los datos financieros clave incluyen gastos en I+D de 2.2 millones de dólares, gastos en marketing de 1.8 millones de dólares y una pérdida neta de 5.0 millones de dólares. La posición de caja era de 16.6 millones de dólares al 30 de septiembre de 2024. La compañía aseguró una colaboración estratégica con Shalby para ensayos clínicos multicéntricos en India y fue nombrada Compañía de Reemplazo Articular Ortopédico del Año 2024.

모노그램 테크놀로지스(NASDAQ:MGRM)는 2024년 3분기 재무 결과를 보고하며 1300만 달러 규모의 확대된 공모를 달성했다고 강조했습니다. 이 회사는 mBȏs TKA 시스템에 대한 510(k) 사전 시장 제출을 했으며, FDA로부터 추가 정보 요청을 받았습니다. 주요 재무 사항에는 220만 달러의 연구개발비, 180만 달러의 마케팅 비용, 500만 달러의 순손실이 포함됩니다. 2024년 9월 30일 기준 현금 잔고는 1660만 달러였습니다. 이 회사는 인도에서 다중 센터 임상 시험을 위한 샬비와 전략적 협업을 확보했고, 2024년 정형외과 관절 치환 회사로 선정되었습니다.

Monogram Technologies (NASDAQ:MGRM) a annoncé les résultats financiers du troisième trimestre 2024, mettant en avant une augmentation et une sursouscription d'une offre publique de 13 millions de dollars. L'entreprise a déposé une demande de précommercialisation 510(k) pour son système mBȏs TKA et a reçu une Demande d'Informations Supplémentaires de la FDA. Les principaux indicateurs financiers comprennent des dépenses en R&D de 2,2 millions de dollars, des dépenses marketing de 1,8 million de dollars, et une perte nette de 5,0 millions de dollars. La position de liquidités s'élevait à 16,6 millions de dollars au 30 septembre 2024. L'entreprise a sécurisé une collaboration stratégique avec Shalby pour des essais cliniques multicentriques en Inde et a été nommée Société de Remplacement Articulaire Orthopédique de l'Année 2024.

Monogram Technologies (NASDAQ:MGRM) berichtete über die Finanzergebnisse des dritten Quartals 2024 und hob ein erhöhtes und überzeichnetes öffentliches Angebot von 13 Millionen Dollar hervor. Das Unternehmen reichte einen 510(k) Vorantrag für sein mBȏs TKA-System ein und erhielt eine Zusätzliche Informationsanfrage von der FDA. Wichtige Finanzkennzahlen umfassen F&E-Ausgaben von 2,2 Millionen Dollar, Marketingausgaben von 1,8 Millionen Dollar und einen Nettoverlust von 5,0 Millionen Dollar. Die Liquiditätsposition betrug zum Stichtag 30. September 2024 16,6 Millionen Dollar. Das Unternehmen sicherte sich eine strategische Zusammenarbeit mit Shalby für multilaterale klinische Studien in Indien und wurde als Orthopädisches Gelenkersatzunternehmen des Jahres 2024 ausgezeichnet.

Positive
  • Secured $13 million through oversubscribed public offering
  • Strategic collaboration with Shalby for clinical trials in India
  • Cash position increased to $16.6 million from $13.6 million in December 2023
  • R&D expenses decreased to $2.2 million from $2.7 million year-over-year
Negative
  • Net loss increased to $5.0 million from $1.0 million year-over-year
  • Marketing expenses significantly increased to $1.8 million from $32,220 year-over-year
  • FDA placed 510(k) application on hold pending Additional Information Request response

Insights

The Q3 results reveal significant financial developments, with a notable $13 million oversubscribed public offering strengthening the balance sheet. The cash position improved to $16.6 million, up from $13.6 million at year-end 2023. However, the $5.0 million net loss represents a concerning increase from the $1.0 million loss in the prior year, primarily due to elevated marketing expenses of $1.8 million related to the Series D offering.

R&D expenses decreased to $2.2 million from $2.7 million, reflecting completion of key development milestones. The cash runway appears sufficient for near-term commercialization goals, though careful monitoring of burn rate is warranted given the regulatory uncertainties ahead.

The FDA review process shows typical progression with some key challenges. The Additional Information Request (AIR) received is not unusual, as 68% of 510(k) applications face similar requests. The 28,000-page submission complexity likely contributed to this outcome. The planned December issue-specific meeting with FDA will be important for determining the timeline to potential clearance.

The strategic pivot to pursue OUS clinical trials in India with Shalby represents a smart parallel path to gather clinical data. The planned 92-patient trial with 3-month follow-up could provide valuable safety and efficacy data to support both international commercialization and potentially strengthen the FDA submission.

Closed an Upsized and Oversubscribed $13 Million Public Offering to Fund Near-term Commercialization Milestones

Management to Host Business Update Conference Call on Tuesday, November 19, 2024 at 4:30 p.m. Eastern Time

AUSTIN, TX / ACCESSWIRE / November 14, 2024 / Monogram Technologies Inc. (NASDAQ:MGRM) ("Monogram" or the "Company"), an AI-driven robotics company focused on improving human health with an initial focus on orthopedic surgery, has reported its financial and operational results for the third quarter ended September 30, 2024.

Third Quarter 2024 and Subsequent Operational Highlights

  • Closed an upsized and oversubscribed $13 million public offering

  • Submitted a 510(k) premarket filing to the U.S. Food and Drug Administration (FDA) for the Company's semi-active version of the mBôs TKA System and passed the FDA Administrative Review.

  • Received an Additional Information Request ("AIR") from the U.S. Food and Drug Administration ("FDA") regarding its 510(k) premarket filing submission for the Company's mBôs TKA System (the "Application").

  • Secured initial strategic collaboration with Shalby Limited ("Shalby"), a global multi-specialty hospital chain and one of India's leading orthopedic hospital groups, to conduct a multicenter clinical trial to demonstrate the safety and effectiveness of the mBȏs TKA System.

  • Named Orthopedic Joint Replacement Company of the Year 2024 by Medical Tech Outlook.

Management Commentary

"The third quarter was highlighted by an upsized and oversubscribed $13 million public offering and continued progress toward clearance for the semi-active version of the mBôs™ TKA System with the FDA," said Ben Sexson, Chief Executive Officer of Monogram. "Funds from the offering are expected to provide the cash runway to meet near-term commercialization milestones and resources to support key initiatives, including clinical trials and further development of our technology.

"We are also working to obtain FDA clearance for our 510(k) submission. The Application was submitted on July 19, 2024, and passed the initial FDA Administrative Review. On September 30, 2024, we received an Additional Information Request ("AIR") from the FDA regarding the submission, placing the application on hold pending a complete response to the AIR within 180 days. According to the 2nd Quarter FY2023 MDUFA V Performance Report, the FDA requested AIR on the first FDA review cycle for approximately 68% of 510(k) applications submitted in FY2022, and given our submission was over 28,000 pages, the AIR aligned with our expectations.

"On October 16, 2024, we held a teleconference with the agency to address clarification questions, which we found constructive. We believe this response provides more transparency for our path forward. The FDA recommended an issue-specific submission (q submission) to discuss our planned approach for responding to the AIR. We anticipate holding the issue-specific meeting with the FDA by December 2024. If the FDA accepts the current planned approach, we believe we could address the AIR within the allotted period; however, this timeline could change based on the outcome of the December issue-specific meeting wherein the FDA may comment on the planned approach.

"As we work to respond to the AIR, we have submitted an application to run an Outside the United States ("OUS") clinical trial on the fully autonomous version of the system in collaboration with Shalby Limited, a global multi-specialty hospital chain and one of India's leading orthopedic hospital groups. This would prepare the groundwork for the international launch of the mBȏs TKA System. Under the collaboration, Shalby will enroll patients at various sites in India for surgeons to evaluate the safety and effectiveness of the mBȏs TKA System with the Consensus CKS implant, which is substantially equivalent to the Monogram mPress implants for regulatory purposes.

"During the quarter, we continued to hold cadaveric system demos, receiving surgeon and market interest for our hands-free, fully active system. With this support, we continue to believe in our thesis for orthopedic robotics and the value proposition of our proposed active robotic system and are confident such a system could be a game-changing advancement for the industry. Validating this thesis, we were recently named ‘Orthopedic Joint Replacement Company of the Year 2024' by Medical Tech Outlook from an expert panel of C-level executives, industry thought leaders, and the editorial board.

"Looking ahead, we are highly focused on the response to the AIR and trying to obtain FDA clearance of our 510(k) submission as quickly and economically as possible. We are working with regulators, our Contract Research Organization (CRO) and the team at Shalby to obtain clearance and plan logistics for our anticipated multicenter clinical trial. We are also exploring further domestic and international relationships as we move toward commercialization. We look forward to additional updates in the weeks and months to come as we execute on our upcoming milestones," concluded Sexson.

Upcoming Milestones

  • Issue-specific meeting with the FDA by December 2024.

  • Obtain regulatory clearance to conduct clinical trials in India with strategic partner Shalby Hospitals.

  • Conduct OUS live-patient surgery trials and submit clinical trial data to FDA, with clinical trials expected to include 92 total knee replacement procedures with a 3-month clinical follow-up.

  • Seek to obtain clearance for the mBôs™ TKA System.

  • Continue exploring domestic relationships.

  • Continue expanding international relationships (the Company will be exhibiting at Arab Health in January 2025).

Third Quarter 2024 Financial Results

Research and development expenses for the third quarter ended September 30, 2024, were $2.2 million, compared to $2.7 million in the prior-year quarter. The R&D decrease was primarily a result of the Company finalizing the validation phase of the verification and validation phase of its robot prototype with the submission of the application for 510 (k) FDA clearance.

Marketing and advertising expenses for the third quarter ended September 30, 2024, were $1.8 million, compared to $32,220 in the prior-year quarter. The increase in marketing and advertising expenses was driven by the marketing campaign to support the Series D preferred Stock Offering which commenced in July 2024 and closed on October 2, 2024.

General & administrative expenses for the third quarter ended September 30, 2024, were $1.1 million compared to $1.1 million in the prior-year quarter.

Net loss of $5.0 million for the third quarter ended September 30, 2024, as compared to a net loss of $1.0 million for the prior-year quarter. The increased loss variance was driven primarily by the increase in marketing expenses in the third quarter ended September 30, 2024 noted above combined with a noncash gain in the third quarter ended September 30, 2023, related to the change in fair market value of a warrant liability that is no longer outstanding.

Cash and cash equivalents totaled $16.6 million as of September 30, 2024, compared to $13.6 million as of December 31, 2023. The company continues to marshal its resources with a focus on commercializing the mBôs™ TKA System as capital efficiently as possible.

Third Quarter 2024 Business Update Conference Call

Monogram Chief Executive Officer Ben Sexson and Chief Financial Officer Noel Knape will host the conference call, followed by a question-and-answer period.

To access the call, please use the following information:

Date:

Tuesday, November 19, 2024

Time:

4:30 p.m. Eastern Time (1:30 p.m. Pacific Time)

Toll-free dial-in number:

1-877-407-9208

International dial-in number:

1-201-493-6784

Conference ID:

13749601

The conference call will be broadcast live and available for replay at https://viavid.webcasts.com/starthere.jsp?ei=1693340&tp_key=7ecb89475b and via the investor relations section of the Company's website here.

About Monogram Technologies Inc.

Monogram Technologies (NASDAQ: MGRM) is an AI-driven robotics company focused on improving human health, with an initial focus on orthopedic surgery. The Company is developing a product solution architecture to enable patient-optimized orthopedic implants at scale by combining 3D printing, advanced machine vision, AI and next-generation robotics.

Monograms mBôs precision robotic surgical system is designed to autonomously execute optimized paths for high-precision insertion of its FDA-cleared mPress press-fit implants. The goal is well balanced better-fitting bone sparing knee replacements. The Company initially intends to produce and market robotic surgical equipment and related software, orthopedic implants, tissue ablation tools, navigation consumables, and other miscellaneous instrumentation necessary for reconstructive joint replacement procedures. Other clinical and commercial applications for the mBôs with mVision navigation are also being explored.

Monogram has obtained FDA clearance for mPress implants and applied for 510(k) clearance for its robotic products. The Company is required to obtain FDA clearance before it can market its products. Monogram cannot estimate the timing or assure the ability to obtain such clearances.

The Company believes that its mBôs precision robotic surgical assistants, which combine AI and novel navigation methods (mVision), will enable more personalized knee implants for patients, resulting in well balanced better-fitting knee replacements with bone sparing implants. Monogram anticipates that there may be other clinical and commercial applications for its navigated mBôs precision robot and mVision navigation.

To learn more, visit www.monogramtechnologies.com.

Forward-Looking Statements

This press release may contain "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. Statements other than statements of historical facts included in this press release may constitute forward-looking statements and are not guarantees of future performance or results and involve a number of risks and uncertainties. For example, the Company's statement regarding the Company's proposed use of net proceeds is a forward-looking statement. Forward-looking statements, other than statements of historical fact, are highly likely to be affected by other unknowable future events and conditions, including elements of the future that are or are not under our control, and that the Company may or may not have considered; accordingly, such statements cannot be guarantees or assurances of any aspect of future performance. Actual developments and results are highly likely to vary materially from any forward-looking statements as a result of a number of factors, including those described in the prospectus and the Company's other filings with the SEC. The Company undertakes no duty to update any forward-looking statement made herein. All forward-looking statements speak only as of the date of this press release.

Investor Relations

Chris Tyson
Executive Vice President
MZ North America
Direct: 949-491-8235
MGRM@mzgroup.us

MONOGRAM ORTHOPAEDICS INC.
CONDENSED BALANCE SHEETS

September 30,

December 31,

2024

2023

(unaudited)

Assets

Current assets:

Cash and cash equivalents

$

16,565,142

$

13,589,028

Account receivable

-

364,999

Prepaid expenses and other current assets

2,065,863

664,262

Total current assets

18,631,005

14,618,289

Equipment, net of accumulated depreciation

829,216

945,020

Intangible assets, net

391,250

548,750

Operating lease right-of-use assets

370,795

466,949

Total assets

$

20,222,266

$

16,579,008

Liabilities and Stockholders' Equity

Current liabilities:

Accounts payable

$

1,536,663

$

2,462,268

Accrued liabilities

874,797

227,684

Operating lease liabilities, current

135,757

128,266

Total current liabilities

2,547,217

2,818,218

Operating lease liabilities, non-current

260,904

363,724

Total liabilities

2,808,121

3,181,942

Commitments and contingencies

-

-

Stockholders' equity:

Series D Preferred Stock, par value $0.0001 per share; 6,000,000 shares authorized; 4,614,453 shares issued and outstanding

4,614

-

Common stock, $.001 par value; 90,000,000 shares authorized; 34,312,261 and 31,338,391shares issued and outstanding at September 30, 2024 and December 31, 2023, respectively

34,312

31,338

Additional paid-in capital

81,083,405

64,874,392

Accumulated deficit

(63,708,186

)

(51,508,664

)

Total stockholders' equity

17,414,145

13,397,066

Total liabilities and stockholders' equity

$

20,222,266

$

16,579,008

MONOGRAM ORTHOPAEDICS INC.
CONDENSED STATEMENTS OF OPERATIONS (UNAUDITED)

Three months ended

Nine months ended

September 30,

September 30,

2024

2023

2024

2023

Product revenue

$

-

$

-

-

-

Cost of goods sold

-

-

$

-

$

-

Gross profit

-

-

-

-

Operating expenses:

Research and development

2,214,729

2,664,542

7,047,112

7,577,907

Marketing and advertising

1,838,937

32,220

2,050,347

2,844,748

General and administrative

1,093,456

1,060,270

3,293,344

2,968,644

Total operating expenses

5,147,122

3,757,032

12,390,803

13,391,299

Loss from operations

(5,147,122

)

(3,757,032

)

(12,390,803

)

(13,391,299

)

Other income:

Change in fair value of warrant liability

-

2,646,399

-

3,088,533

Interest income and other, net

112,621

114,973

312,142

211,843

Total other income

112,621

2,761,372

312,142

3,300,376

Net loss before taxes

(5,034,501

)

(995,660

)

(12,078,661

)

(10,090,923

)

Income taxes

-

-

-

-

Net loss

$

(5,034,501

)

$

(995,660

)

$

(12,078,661

)

$

(10,090,923

)

Basic and diluted loss per common share

$

(0.16

)

$

(0.03

)

$

(0.38

)

$

(0.52

)

Weighted-average number of basic and diluted shares outstanding

32,223,656

29,284,949

31,806,252

19,482,606

MONOGRAM ORTHOPAEDICS INC.
CONDENSED STATEMENTS OF CASH FLOWS (UNAUDITED)

Nine months ended

September 30,

2024

2023

Operating activities:

Net loss

$

(12,078,661

)

$

(10,090,923

)

Adjustments to reconcile net loss to net cash used in operating activities:

Stock-based compensation

942,528

1,158,499

Other expenses settled with stock issuances

50,000

80,000

Loss from change in fair value of common stock make-whole obligation

35,749

-

Depreciation and amortization

321,114

307,293

Change in fair value of warrant liability

-

(3,088,533

)

Changes in non-cash working capital balances:

Account receivable

364,999

-

Other current assets

(168,691

)

273,079

Accounts payable

(925,605

)

1,121,822

Accrued liabilities

490,504

(197,243

)

Operating lease assets and liabilities, net

825

5,622

Cash used in operating activities

(10,967,238

)

(10,430,384

)

Investing activities:

Purchases of equipment

(47,809

)

(40,765

)

Cash used in investing activities

(47,809

)

(40,765

)

Financing activities:

Proceeds from issuances of Common Stock, net of cash costs

4,177,931

15,254,300

ELOC issuance cost

-

(523,362

)

Proceeds from issuances of Series C Preferred Stock, net

-

147,042

Proceeds from issuances of Series D Preferred Stock, net

9,813,230

-

Cash provided by financing activities

13,991,161

14,877,980

Increase (decrease) in cash and cash equivalents during the period

2,976,114

4,406,831

Cash and cash equivalents, beginning of the period

13,589,028

10,468,645

Cash and cash equivalents, end of the period

$

16,565,142

$

14,875,476

Noncash investing and financing activities:

Receivable from stock offerings' selling agent

$

1,378,867

$

-

Amortization of deferred issuance costs of Common Stock Purchase Agreement

$

145,956

$

-

Series D Preferred Stock dividends payable

$

120,860

$

-

Cashless exercise of warrant

$

246

$

926,335

Common Stock issued for services related to Common Stock Purchase Agreement

$

-

$

247,980

SOURCE: Monogram Technologies Inc.



View the original press release on accesswire.com

FAQ

What was Monogram Technologies (MGRM) net loss in Q3 2024?

Monogram Technologies reported a net loss of $5.0 million for Q3 2024, compared to a net loss of $1.0 million in the prior-year quarter.

How much did MGRM raise in their public offering in Q3 2024?

Monogram Technologies closed an upsized and oversubscribed $13 million public offering in Q3 2024.

What is the current status of MGRM's FDA 510(k) application?

The FDA issued an Additional Information Request (AIR) on September 30, 2024, placing the application on hold. The company must respond within 180 days and plans an issue-specific meeting with FDA by December 2024.

What was MGRM's cash position as of September 30, 2024?

Monogram Technologies reported cash and cash equivalents of $16.6 million as of September 30, 2024.

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