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DNTHDianthus Therapeutics, Inc.Sell5.2·$82.07+7.35%
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Dianthus Therapeutics, Inc. (DNTH) Stock Analysis

Range Bound setup

SellModerate Confidence

Healthcare · Biotechnology

Sell if holding. Engine safety override at $82.07: Quality below floor (3.1 < 4.0) triggers a hard block regardless of the otherwise-positive setup — overall score 5.2/10 and A.R:R 2.4:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 14%; Elevated put/call ratio: 1.57; Below-average business quality.

Dianthus Therapeutics is a clinical-stage biotech developing complement inhibitors for severe autoimmune diseases, with claseprubart (C1s inhibitor) in Phase 3 for CIDP and Phase 2 for gMG and MMN, plus DNTH212 (BDCA2/BAFF-APRIL inhibitor) in Phase 1. The company has no approved... Read more

$82.07+35.3% A.UpsideScore 5.2/10#82 of 157 Biotechnology
QualityF-score4 / 9FCF yield-1.58%
Stop $76.33Target $111.07(analyst − 13%)A.R:R 2.4:1
Analyst target$127.67+55.6%12 analysts
$111.07our TP
$82.07price
$127.67mean
$200

Sell if holding. Engine safety override at $82.07: Quality below floor (3.1 < 4.0) triggers a hard block regardless of the otherwise-positive setup — overall score 5.2/10 and A.R:R 2.4:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 14%; Elevated put/call ratio: 1.57; Below-average business quality. Chart setup: RSI 45 mid-range, Bollinger mid-band. Score 5.2/10, moderate confidence.

Passes 6/7 gates (favorable risk/reward ratio, clean insider activity, no SEC red flags, earnings proximity 54d clear, semi cycle peak clear, materials cycle peak clear). Fails on weak momentum. Suitability: aggressive.

10-K grounded · weekly refresh

About Dianthus Therapeutics, Inc.

About Dianthus Therapeutics, Inc.

Dianthus Therapeutics' lead clinical candidate, claseprubart, is a selective C1s complement inhibitor running in three active trials: a Phase 3 CIDP program (CAPTIVATE) that achieved its interim responder-rate target in March 2026, a Phase 2 gMG program (MaGic) reporting positive top-line data in September 2025, and a Phase 2 MMN program (MoMeNtum) with top-line results expected in the second half of 2026. Net losses reached $162.3 million in 2025, up from $85.0 million in 2024.

Dianthus earns no product revenue and funds operations entirely through equity issuances. In September 2025, the company completed an underwritten public offering issuing 7,627,879 shares of common stock plus pre-funded warrants to purchase up to 1,112,121 shares; management has also sold 2,626,834 shares under an at-the-market program. Based on its current operating plan, Dianthus believes existing cash, equivalents, and investments will fund operations into 2028. Claseprubart is manufactured through contract development and manufacturing organizations. A second clinical candidate, DNTH212—a bifunctional BDCA2 and BAFF/APRIL inhibitor licensed from Nanjing Leads Biolabs Co., Ltd. on October 16, 2025—entered a Phase 1 study in December 2025 in healthy volunteers and systemic lupus erythematosus patients in China, with top-line healthy volunteer data expected in the second half of 2026. Competitors in gMG include argenx's efgartigimod (Vyvgart/Vyvgart Hytrulo, FDA-approved 2021/2023) and C5 inhibitors eculizumab (Soliris) and ravulizumab (Ultomiris); in CIDP, Vyvgart Hytrulo gained approval in June 2024.

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The entirety of Dianthus' near-term value rests on a pivotal Phase 3 readout in CIDP: following the March 2026 CAPTIVATE interim analysis, the company plans to seek regulatory approval to revise the study design and intends to file a Biologics License Application in adult CIDP patients if the trial succeeds. A second binary event is the Phase 3 gMG trial, expected to initiate in mid-2026 with top-line results anticipated in the second half of 2028—a timeline that consumes a significant portion of the company's estimated cash runway through 2028.

See also: Healthcare · Biotechnology

From Dianthus Therapeutics, Inc.'s most recent 10-K filing, extracted June 9, 2026.

news + 30-day 8-K events · 5-min refresh

Recent developments

updated 2026-06-13

Recent Developments — Dianthus Therapeutics, Inc.

Generated 2026-06-15T18:11:46Z.

TrendMatrix Research · upcoming catalyst calendar

Upcoming dated catalysts

Thu, Aug 6, 202654d to earnings· next earnings call

Thesis

Rewards
No bull case signals
Risks
Concentration risk — Pipeline: claseprubart
Quality below floor (3.1 < 4.0)

Key Metrics

P/E (TTM)
P/E (Fwd)-17.6
Mkt Cap$4.5B
EV/EBITDA-17.7
Profit Mgn0.0%
ROE-22.7%
Rev Growth-60.2%
Beta0.07
DividendNone
Rating analysts22

Quality Signals

Piotroski F4/9MoatNarrow

Options Flow

P/C1.57bearish
IV88%elevated
Max Pain$75-8.6% vs spot

Concentration Risks(10-K Item 1A)

  • HIGHpipelineclaseprubart
    10-K Item 1A: 'We are substantially dependent on the success of our most advanced product candidate, claseprubart'

Model-generated analysis — not investment advice. Not a registered investment advisor. Past performance does not guarantee future results.

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Performance. Past performance is not indicative of future results. Performance figures reflect the published model only and do not reflect any individual subscriber's actual results.

Methodology · Editorial policy & full disclaimer

Rating Breakdown

3 floor-breakers·1 ceiling hit

Quality below the gate floor. Component breakdown shows what dragged the score down.static

Roe
0.0
Roa
0.0
Net Margin
0.0
Fcf Quality
0.0
Rule Of 40
3.0
Piotroski F
4.4
Current Ratio
5.0
Moat
5.5
Gross Margin
10.0
Cash-burning: FCF -5317% of revenueRule of 40: -5377 (fail)

Momentum below the gate floor. Component breakdown shows what dragged the score down.static

Macd
0.0
Obv
1.0
Ma Position
4.0
Rsi
5.5
Volume
6.3
Volume distribution (falling OBV)Above 200-day MA

No near-term catalyst priced in. Thesis progression will come from fundamentals grinding, not event reaction.static

Earnings History
0.0
Surprise Avg
0.0
Erm
5.0
Earnings Timing
5.0
News Activity
8.0
Earnings concerns: 1B/3M
GatesMomentum 3.4<4.5A.R:R 2.4 ≥ 1.5Insider activity: OKNo SEC red flagsEARNINGS PROXIMITY 54d clearSEMI CYCLE PEAK CLEARMATERIALS CYCLE PEAK CLEARRange BoundSuitability: Aggressive
RSI
45 · Neutral
20D MA 50D MA 200D MAGOLDEN CROSSSupport $68.85Resistance $93.61

Price Targets

$76
$111
A.Upside+35.3%
A.R:R2.4:1

Position Sizing

ConvictionNone
Suggested %0.5%
Max %1%
RegimeSteady

Risk Alerts

! Quality below floor (3.1 < 4.0)
! momentum at 3.4 (below the engine's 4.5 threshold)

Earnings

B
M
M
M
1/4 beats
Next Earnings2026-08-06 (54d)

Verdict History

reverse chrono — latest first
Loading history...
Verdicts are recorded on every nightly pipeline run. Rows capture transitions (verdict flips, score deltas ≥0.3, entry/TP/SL changes). Rows with a ▶ can be expanded to see the change reason. Aggregate cohort performance is tracked in the recommendation ledger.
Frequently Asked Questions
Is DNTH stock a buy right now?

Sell if holding. Engine safety override at $82.07: Quality below floor (3.1 < 4.0) triggers a hard block regardless of the otherwise-positive setup — overall score 5.2/10 and A.R:R 2.4:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 14%; Elevated put/call ratio: 1.57; Below-average business quality. Chart setup: RSI 45 mid-range, Bollinger mid-band. Prior stop was $76.33. Score 5.2/10, moderate confidence.

What is the DNTH stock price target?

Take-profit target: $111.07 (+35.3% upside). Prior stop was $76.33. Stop-loss: $76.33.

What are the risks of investing in DNTH?

Concentration risk — Pipeline: claseprubart; Quality below floor (3.1 < 4.0).

Is DNTH overvalued or undervalued?

Dianthus Therapeutics, Inc. trades at a P/E of N/A (forward -17.6). TrendMatrix value score: 9.0/10. Verdict: Sell.

What do analysts say about DNTH?

22 analysts cover DNTH with a consensus score of 4.4/5. Average price target: $128.

What does Dianthus Therapeutics, Inc. do?Dianthus Therapeutics is a clinical-stage biotech developing complement inhibitors for severe autoimmune diseases, with...

Dianthus Therapeutics is a clinical-stage biotech developing complement inhibitors for severe autoimmune diseases, with claseprubart (C1s inhibitor) in Phase 3 for CIDP and Phase 2 for gMG and MMN, plus DNTH212 (BDCA2/BAFF-APRIL inhibitor) in Phase 1. The company has no approved products and reported net losses of $162.3 million in 2025 and $85.0 million in 2024.

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