Kyverna Therapeutics Inc

Aktienanalyse zu Kyverna Therapeutics Inc (KYTX)

$5.390

-0.320 (-5.93%)Zum Schluss

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Hoch
5.730
Eröffnung
5.650
Volumengewichteter Durchschnittskurs
5.49
Volumen
827.03K
Marktkap.
—
Tief
5.360
Umsatz
4.54M
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

KI-Analyse of Kyverna Therapeutics Inc (KYTX)

Verkaufen

Kyverna Therapeutics Inc is not a good buy right now due to its current price of $5.67, which is significantly below the analyst price targets of $25 and $29. However, the stock has seen a 35.35% decline year-to-date, indicating potential for recovery. The RSI is at 29.778, suggesting the stock is oversold, but the negative earnings trend with a forward P/E of 0 and consistent losses (latest EPS reported at -0.63) raises concerns about its financial health. The main risk is the ongoing net losses, with a net income of -39,728,000 USD in Q1 2026, which could hinder future growth and recovery.

Bewertungskennzahlen

Das aktuelle erwartete KGV von Kyverna Therapeutics Inc (KYTX) beträgt 0.00, verglichen mit dem 5-Jahres-Durchschnitt von -2.51.

Erwartetes KGV

Überbewertet
5J-Durchschnitt P/E
-2.51
Aktuelles P/E
0.00
Überbewertet
-0.21
Unterbewertet
-4.81

Erwartetes EV/EBITDA

Fair bewertet
5J-Durchschnitt EV/EBITDA
-0.89
Aktuelles EV/EBITDA
0.00
Überbewertet
1.98
Unterbewertet
-3.77

Erwartetes KUV

Fair bewertet
5J-Durchschnitt P/S
9.52
Aktuelles P/S
21.00
Überbewertet
24.43
Unterbewertet
-5.39

Alphio-AI-Kursszenarien für KYTX

Szenariopreise sind das letzte monatliche Prognoseband des laufenden Jahres. Die Wahrscheinlichkeiten sind feste Modellgewichte (25 / 50 / 25), keine Garantien.

B

Bullisch

Bullisch · 25%KYTX

$4.24

Szenariopreis

B

Basis

Basis · 50%KYTX

$3.52

Szenariopreis

B

Bärisch

Bärisch · 25%KYTX

$3.43

Szenariopreis

Whales, die KYTX halten

I

Insight Venture Management, LLC

+ HältKYTX

+6.37%

3-Monats-Rendite

G

Gilead Sciences, Inc.

+ HältKYTX

-26.12%

3-Monats-Rendite

Event-Zeitleiste

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

News

KYTX FAQ – beantwortet von 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 its current price of $5.67, which is significantly below the analyst price targets of $25 and $29. However, the stock has seen a 35.35% decline year-to-date, indicating potential for recovery. The RSI is at 29.778, suggesting the stock is oversold, but the negative earnings trend with a forward P/E of 0 and consistent losses (latest EPS reported at -0.63) raises concerns about its financial health. The main risk is the ongoing net losses, with a net income of -39,728,000 USD in Q1 2026, which could hinder future growth and recovery.

Community

Mehr ↗
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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