Dianthus Therapeutics Highlights Recent Business Achievements and Reports Q4 and FY 2024 Financial Results

Rhea-AI Summary

Dianthus Therapeutics (DNTH) has reported its Q4 and FY 2024 financial results, highlighting significant progress in its clinical trials. The company's lead candidate DNTH103, a monoclonal antibody targeting the classical complement pathway, is advancing in multiple trials:

- Phase 2 MaGic trial in generalized Myasthenia Gravis (gMG) with top-line results expected in 2H'25
- Phase 3 CAPTIVATE trial in Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) with interim analysis in 2H'26
- Phase 2 MoMeNtum trial in Multifocal Motor Neuropathy (MMN) with results expected in 2H'26

Financial highlights include:
- Cash position of $357.0 million providing runway into 2H'27
- R&D expenses increased to $83.1 million in 2024
- Net loss of $85.0 million or $2.55 per share
- G&A expenses reached $25.0 million

Positive

• Strong cash position of $357.0M providing extended runway into 2H'27
• Multiple clinical trial milestones expected in 2025-2026
• Potential for single pivotal trial to support BLA filing for CIDP indication

Negative

• Net loss increased to $85.0M in 2024 from $43.6M in 2023
• R&D expenses significantly increased to $83.1M from $32.8M year-over-year
• G&A expenses rose to $25.0M from $18.2M in previous year

Insights

Financial Analyst

Dianthus Therapeutics' Q4 and FY2024 results reflect a company executing methodically across its clinical pipeline while maintaining a strong financial position. The $357 million cash runway extending into 2H'27 provides significant operational flexibility as the company advances its lead candidate DNTH103 through multiple clinical trials, including a Phase 3 study in CIDP.

The financial metrics show the expected pattern of a clinical-stage biotech with increasing investments. R&D expenses more than doubled year-over-year to $83.1 million (from $32.8 million), reflecting the company's advancement into later-stage trials across three indications. Net loss widened to $85.0 million, though loss per share improved to $2.55 from $8.45 previously, likely reflecting an increased share count following financing activities.

While no near-term catalysts exist before the 2H'25 readout from the Phase 2 gMG trial, DNTH103's differentiated profile as a selective C1s inhibitor with convenient subcutaneous dosing potential positions the company well in the competitive complement inhibitor landscape. The appointment of a Chief Commercial Officer suggests forward-looking preparation, though commercial revenue remains years away.

For investors, the key value proposition centers on DNTH103's potential as a "pipeline-in-a-product" across multiple autoimmune indications. The absence of trial delays, combined with sufficient funding through multiple data readouts, provides a stable foundation for execution. However, with no near-term catalysts, investor patience will be required as the clinical data matures across 2025-2026.

Phase 2 MaGic trial of DNTH103 in generalized Myasthenia Gravis (gMG) ongoing; top-line results on track for 2H’25

Phase 3 CAPTIVATE trial of DNTH103 in Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) ongoing; interim responder analysis anticipated in 2H’26

Phase 2 MoMeNtum trial of DNTH103 in Multifocal Motor Neuropathy (MMN) ongoing;
top-line results anticipated in 2H’26

$357.0 million of cash provides runway into 2H’27

NEW YORK and WALTHAM, Mass., March 11, 2025 (GLOBE NEWSWIRE) -- Dianthus Therapeutics, Inc. (Nasdaq: DNTH), a clinical-stage biotechnology company dedicated to advancing the next generation of antibody complement therapeutics to treat severe autoimmune diseases, today reported financial results for the fourth quarter and full year ending December 31, 2024 and provided an update on recent business achievements.

“We remain on track to report top-line data in 2H’25 from our Phase 2 clinical trial of DNTH103 in gMG, an indication where a best-in-class, potent active C1s and classical pathway inhibitor with the potential for effective and consistent symptom control along with improved safety and convenience could meaningfully advance the standard of care,” said Marino Garcia, Chief Executive Officer of Dianthus Therapeutics. “We are excited to have initiated our pivotal Phase 3 CAPTIVATE trial in CIDP, which is on track for an interim responder analysis in 2H’26, along with top-line results from our Phase 2 trial in MMN.”

DNTH103 Clinical Development

DNTH103 is an investigational, clinical-stage, potent monoclonal antibody engineered to selectively target the classical pathway by inhibiting only the active form of the C1s protein, a clinically validated complement target. DNTH103 is enhanced with YTE half-life extension technology designed to enable a more convenient subcutaneous, self-administered injection dosed as infrequently as once every two weeks. DNTH103 has the potential to be a best-in-class pipeline-in-a-product across a range of autoimmune disorders with high unmet need.

Generalized Myasthenia Gravis (gMG)

• Phase 2 MaGic gMG trial ongoing: The MaGic trial is a global, randomized, double-blind, placebo-controlled Phase 2 trial in patients with gMG who are acetylcholine receptor (AChR) antibody positive, and it remains on track to report top-line results in 2H’25.
  

Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

• Phase 3 CAPTIVATE CIDP trial ongoing: The CAPTIVATE trial is a single, global, two-part, randomized withdrawal Phase 3 trial in patients with CIDP, and it remains on track for an interim responder analysis in 2H’26. The Company believes this single pivotal trial will support a BLA filing in adult patients with CIDP.
  

Multifocal Motor Neuropathy (MMN)

• Phase 2 MoMeNtum MMN trial ongoing: The MoMeNtum trial is a global, randomized, double-blind, placebo-controlled Phase 2 trial in patients with MMN, and it remains on track to report top-line results in 2H’26.
  

Corporate Updates

• On March 5, 2025, John C. King was announced as Chief Commercial Officer and Sujay Kango joined the Company’s Board of Directors. Mr. King brings to Dianthus more than 25 years of global commercial leadership experience in biotechnology, including neuromuscular and hematological rare diseases. Mr. Kango is an experienced executive with more than 26 years of experience in the pharmaceutical and biotechnology sector.
  

Full Year 2024 Financial Results

• Cash Position - $357.0 million of cash, cash equivalents and investments as of December 31, 2024 is projected to provide runway into the second half of 2027.

• R&D Expenses - Research and development (R&D) expenses for the year ended December 31, 2024 were $83.1 million, inclusive of $5.6 million of stock-based compensation, compared to $32.8 million for the year ended December 31, 2023, which included $0.9 million of stock-based compensation. This increase in R&D expenses was primarily driven by higher clinical costs, chemistry, manufacturing and controls (CMC) costs and increased headcount to support DNTH103 Phase 2 and Phase 3 development.

• G&A Expenses - General and administrative (G&A) expenses for the year ended December 31, 2024 totaled $25.0 million, inclusive of stock-based compensation of $7.3 million, compared to $18.2 million for the year ended December 31, 2023, which included $2.0 million of stock-based compensation. This increase in G&A expenses was primarily due to increased headcount and higher professional services costs.

• Net Loss - Net loss for the year ended December 31, 2024 was $85.0 million or $2.55 per share (basic and diluted) compared to $43.6 million or $8.45 per share (basic and diluted) for the year ended December 31, 2023.

• Additional Information - For additional information on the Company’s financial results for the year ended December 31, 2024, please refer to the Form 10-K filed with the SEC.
  

About DNTH103
DNTH103 is an investigational, clinical-stage, potent monoclonal antibody engineered to selectively target the classical pathway by inhibiting only the active form of the C1s protein, a clinically validated complement target. DNTH103 is enhanced with YTE half-life extension technology designed to enable a more convenient subcutaneous, self-administered injection dosed as infrequently as once every two weeks. Additionally, selective inhibition of the classical complement pathway may lower patient risk of infection from encapsulated bacteria by preserving immune activity of the lectin and alternative pathways. As the classical pathway plays a significant role in disease pathology, DNTH103 has the potential to be a best-in-class pipeline-in-a-product across a range of autoimmune disorders with high unmet need. Dianthus is building a neuromuscular franchise with DNTH103 and anticipates reporting top-line data from the Phase 2 MaGic trial in generalized Myasthenia Gravis in 2H’25, the interim responder analysis of the Phase 3 CAPITIVATE trial in Chronic Inflammatory Demyelinating Polyneuropathy in 2H’26, and top-line data from the Phase 2 MoMeNtum trial in Multifocal Motor Neuropathy in 2H’26.

DNTH103 is an investigational agent that is not approved as a therapy in any indication in any jurisdiction worldwide.

About Dianthus Therapeutics
Dianthus Therapeutics is a clinical-stage biotechnology company dedicated to designing and delivering novel, best-in-class monoclonal antibodies with improved selectivity and potency. Based in New York City and Waltham, Mass., Dianthus is comprised of an experienced team of biotech and pharma executives who are leading the development of next-generation antibody complement therapeutics, aiming to deliver transformative medicines for people living with severe autoimmune and inflammatory diseases.

To learn more, please visit www.dianthustx.com and follow us on LinkedIn. 

Cautionary Statement Regarding Forward-Looking Statements
Certain statements in this press release, other than purely historical information, may constitute “forward-looking statements” within the meaning of the federal securities laws, including for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995, express or implied statements regarding future plans and prospects, including statements regarding the expectations or plans for discovery, preclinical studies, clinical trials and research and development programs, in particular with respect to DNTH103, and any developments or results in connection therewith, including the target product profile of DNTH103; the anticipated timing of the initiation and results from those studies and trials; expectations regarding the time period over which the Company’s capital resources are expected to be sufficient to fund its anticipated operations; and expectations regarding the market and potential opportunities for complement therapies, in particular with respect to DNTH103. The words “opportunity,” “potential,” “milestones,” “runway,” “will,” “anticipate,” “achieve,” “near-term,” “catalysts,” “pursue,” “pipeline,” “believe,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “might,” “plan,” “possible,” “predict,” “project,” “should,” “strive,” “would,” “aim,” “target,” “commit,” and similar expressions (including the negatives of these terms or variations of them) generally identify forward-looking statements, but the absence of these words does not mean that statement is not forward looking.

Actual results could differ materially from those included in the forward-looking statements due to various factors, risks and uncertainties, including, but not limited to, that preclinical testing of DNTH103 and data from clinical trials may not be predictive of the results or success of ongoing or later clinical trials, that the development of DNTH103 or the Company's other compounds may take longer and/or cost more than planned, that the Company may be unable to successfully complete the clinical development of the Company’s compounds, that the Company may be delayed in initiating, enrolling or completing its planned clinical trials, and that the Company's compounds may not receive regulatory approval or become commercially successful products. These and other risks and uncertainties are identified under the heading "Risk Factors" included in the Company’s Annual Report on Form 10-K for the period ended December 31, 2024, and other filings that the Company has made and may make with the SEC in the future. Nothing in this press release should be regarded as a representation by any person that the forward-looking statements set forth herein will be achieved or that any of the contemplated results of such forward-looking statements will be achieved.

The forward-looking statements in this press release speak only as of the date they are made and are qualified in their entirety by reference to the cautionary statements herein. Dianthus undertakes no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events or otherwise, except as required by law.

Contact
Jennifer Davis Ruff
Dianthus Therapeutics
jdavisruff@dianthustx.com

Dianthus Therapeutics, Inc.
Consolidated Balance Sheets
(in thousands, except share and per share data) (unaudited)
ASSETS	December 31, 2024				December 31, 2023
Current assets:
Cash and cash equivalents	$	22,792			$	132,325
Short-term investments		252,449				41,393
Receivable from related party		807				294
Unbilled receivable from related party		—				184
Prepaid expenses and other current assets		4,856				3,255
Total current assets		280,904				177,451
Long-term investments		81,728				—
Property and equipment, net		194				185
Right-of-use operating lease assets		1,553				615
Other assets and restricted cash		9,629				1,154
Total assets	$	374,008			$	179,405
LIABILITIES AND STOCKHOLDERS’ EQUITY
Current liabilities:
Accounts payable	$	4,579			$	2,610
Accrued expenses		13,074				6,504
Current portion of deferred revenue		479				—
Current portion of deferred revenue – related party		—				100
Current portion of operating lease liabilities		320				417
Total current liabilities		18,452				9,631
Deferred revenue		1,908				—
Deferred revenue – related party		—				736
Long-term operating lease liabilities		1,171				168
Total liabilities		21,531				10,535
Commitments and contingencies
Stockholders' equity:
Preferred stock		—				—
Common stock		31				15
Additional paid-in capital		526,732				258,231
Accumulated deficit		(174,392	)			(89,423	)
Accumulated other comprehensive income		106				47
Total stockholders' equity		352,477				168,870
Total liabilities and stockholders' equity	$	374,008			$	179,405

Dianthus Therapeutics, Inc.
Consolidated Statements of Operations and Comprehensive Loss
(in thousands, except share and per share data) (unaudited)
	Three Months Ended December 31,								Year Ended December 31,
		2024				2023				2024				2023
Revenues:
License revenue – related party	$	999			$	457			$	5,909			$	2,826
License revenue		326				—				326				—
Total revenues		1,325				457				6,235				2,826
Operating expenses:
Research and development		26,413				8,781				83,105				32,841
General and administrative		6,828				4,632				24,994				18,159
Total operating expenses		33,241				13,413				108,099				51,000
Loss from operations		(31,916	)			(12,956	)			(101,864	)			(48,174	)
Other income/(expense):
Interest income		3,991				2,444				17,365				4,764
Gain/(loss) on investment in related party		(160	)			—				148				—
Gain/(loss) on currency exchange, net		27				(32	)			(64	)			(85	)
Other expense		(380	)			(19	)			(554	)			(60	)
Total other income		3,478				2,393				16,895				4,619
Net loss	$	(28,438	)		$	(10,563	)		$	(84,969	)		$	(43,555	)
Net loss per share attributable to common stockholders, basic and diluted	$	(0.81	)		$	(0.71	)		$	(2.55	)		$	(8.45	)
Weighted-average number of shares of common stock outstanding, used in computing net loss per share of common stock, basic and diluted		35,033,773				14,817,676				33,313,849				5,153,423
Comprehensive loss:
Net Loss	$	(28,438	)		$	(10,563	)		$	(84,969	)		$	(43,555	)
Other comprehensive income/(loss):
Unrealized gains/(losses) on marketable securities		(575	)			51				59				208
Total other comprehensive income/(loss)		(575	)			51				59				208
Total comprehensive loss	$	(29,013	)		$	(10,512	)		$	(84,910	)		$	(43,347	)

FAQ

What are the key milestones for DNTH103's clinical trials in 2025-2026?

DNTH will report Phase 2 gMG trial results in 2H'25, Phase 3 CIDP interim analysis in 2H'26, and Phase 2 MMN trial results in 2H'26.

How much cash does DNTH have and how long will it last?

Dianthus has $357.0 million in cash, providing runway into second half of 2027.

What was DNTH's net loss per share for fiscal year 2024?

Net loss was $85.0 million or $2.55 per share, compared to $43.6 million or $8.45 per share in 2023.

What are the main indications being targeted by DNTH103?

DNTH103 is being developed for generalized Myasthenia Gravis (gMG), Chronic Inflammatory Demyelinating Polyneuropathy (CIDP), and Multifocal Motor Neuropathy (MMN).