Kyverna Therapeutics Inc

Análisis de la acción Kyverna Therapeutics Inc (KYTX)

$5.390

-0.320 (-5.93%)Al cierre

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Máximo
5.680
Apertura
5.680
Precio medio ponderado por volumen
5.48
Volumen
827.75K
Capitalización
—
Mínimo
5.360
Importe
4.53M
EV/EBITDA, TTM
0.00

Kyverna Therapeutics, Inc. is a clinical-stage biopharmaceutical company focused on developing cell therapies for patients with autoimmune diseases. The Company’s lead chimeric antigen receptor (CAR) T-cell therapy candidate, KYV-101, is advancing through clinical development with Phase II trials for stiff person syndrome and myasthenia gravis, and two ongoing multi-center Phase I/II trials for patients with lupus nephritis. KYV-101 is an autologous, fully human CD19 CAR T-cell product candidate incorporating highly potent CD28 co-stimulation. The Company is also harnessing investigator-initiated trials and other KYSA studies, including in multiple sclerosis and systemic sclerosis, to inform the next priority indications for the Company to advance into late-stage development. Its pipeline includes next generation CAR T-cell therapies in both autologous and allogeneic formats with properties intended to be well suited for use in B cell-driven autoimmune diseases.

kyvernatx.com

Análisis de IA of Kyverna Therapeutics Inc (KYTX)

Vender

Kyverna Therapeutics Inc is not a good buy right now due to significant financial losses and negative momentum. The current price is $5.39, and the stock has a 1-year change of -30.99%. Furthermore, the RSI is at 27.395, indicating oversold conditions, but the overall trend remains negative. The company reported a net loss of $39,728,000 in Q1 2026, and the forward P/E is at 0, suggesting no earnings growth in the near term. The main risk is the ongoing investigations into corporate governance breaches, which could further impact investor confidence.

Métricas de valoración

El PER previsto actual de Kyverna Therapeutics Inc (KYTX) es 0.00, frente a su media de 5 años de -2.51.

PER previsto

Sobrevalorado
Media 5A P/E
-2.51
P/E actual
0.00
Sobrevalorada
-0.21
Infravalorada
-4.81

EV/EBITDA previsto

Valor razonable
Media 5A EV/EBITDA
-0.89
EV/EBITDA actual
0.00
Sobrevalorada
1.98
Infravalorada
-3.77

Precio/ventas previsto

Valor razonable
Media 5A P/S
9.54
P/S actual
20.61
Sobrevalorada
24.45
Infravalorada
-5.37

Escenarios de precio de Alphio AI para KYTX

Los precios por escenario son la última banda de previsión mensual del año en curso. Las probabilidades son pesos fijos del modelo (25 / 50 / 25), no garantías.

A

Alcista

Alcista · 25%KYTX

$4.24

Precio del escenario

B

Base

Base · 50%KYTX

$3.52

Precio del escenario

B

Bajista

Bajista · 25%KYTX

$3.43

Precio del escenario

Ballenas con KYTX en cartera

I

Insight Venture Management, LLC

+ Con en carteraKYTX

+6.09%

Rentabilidad a 3 meses

G

Gilead Sciences, Inc.

+ Con en carteraKYTX

-28.74%

Rentabilidad a 3 meses

Cronología de eventos

2026-10-23 (ET)

11:00:00

Kyverna Therapeutics Updates miv-cel Clinical Trial Data

2026-09-24 (ET)

06:30:00

Kyverna Therapeutics Reports Positive One-Year Data from KYSA-8

2026-08-11 (ET)

16:30:00

Kyverna Advances BLA Submission and Clinical Trials

2026-07-27 (ET)

08:30:00

Kyverna and ElevateBio Sign Manufacturing Agreement for miv-cel

2026-07-13 (ET)

09:00:00

Cue Biopharma Appoints Dominic Borie as Chief Medical Officer

Noticias

Preguntas frecuentes sobre KYTX, respondidas por Alphio AI

Kyverna Therapeutics, Inc. is a clinical-stage biopharmaceutical company focused on developing cell therapies for patients with autoimmune diseases. The Company’s lead chimeric antigen receptor (CAR) T-cell therapy candidate, KYV-101, is advancing through clinical development with Phase II trials for stiff person syndrome and myasthenia gravis, and two ongoing multi-center Phase I/II trials for patients with lupus nephritis. KYV-101 is an autologous, fully human CD19 CAR T-cell product candidate incorporating highly potent CD28 co-stimulation. The Company is also harnessing investigator-initiated trials and other KYSA studies, including in multiple sclerosis and systemic sclerosis, to inform the next priority indications for the Company to advance into late-stage development. Its pipeline includes next generation CAR T-cell therapies in both autologous and allogeneic formats with properties intended to be well suited for use in B cell-driven autoimmune diseases. It operates in the Healthcare sector (BIOLOGICAL PRODUCTS, EXCEPT DIAGNOSTIC SUBSTANCES industry).

Kyverna Therapeutics Inc is not a good buy right now due to significant financial losses and negative momentum. The current price is $5.39, and the stock has a 1-year change of -30.99%. Furthermore, the RSI is at 27.395, indicating oversold conditions, but the overall trend remains negative. The company reported a net loss of $39,728,000 in Q1 2026, and the forward P/E is at 0, suggesting no earnings growth in the near term. The main risk is the ongoing investigations into corporate governance breaches, which could further impact investor confidence.

Comunidad

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0xLunarbazaar24/9/2026

$KYTX Swarmer's miv-cel shows positive results in stiff person syndrome and gMG Kyverna Therapeutics announced positive one-year topline data from KYSA-8, its registrational trial of miv-cel - mivocabtagene autoleucel, KYV-101 - in patients with stiff person syndrome or SPS, and positive topline longer-term follow-up data from the Phase 2 portion of KYSA-6, its registrational trial in patients with generalized myasthenia gravis, or gMG. Data from both trials will be shared at upcoming medical meetings. The primary endpoint and all key secondary endpoints were achieved with statistical significance in KYSA-8. The topline one-year durability data further strengthen the positive results. Miv-cel continued to be well-tolerated. Longer-term Phase 2 follow-up in gMG demonstrate robust and durable effects sustained for up to 1.5 years, with majority of patients maintaining MSE. Kyverna intends to include the one-year data in its rolling BLA submission, on track to be completed in Q4. The full data set will be presented at MS Toronto, October 21-23, in Toronto. All 7 patients achieved clinically meaningful improvement in MG-ADL and QMG, co-primary endpoints of the ongoing Phase 3 portion. All 7 patients remained free of immunotherapies for MG. Miv-cel continued to be well-tolerated. The Phase 3 portion of the KYSA-6 trial is ongoing, with enrollment expected to be completed in mid-2027.

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