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Citius Pharmaceuticals, Inc.Informe acción NasdaqCM:CTXR

Capitalización bursátil US$15.7m
Precio de las acciones
US$0.58
US$5
88.4% infravalorado descuento intrínseco
1Y-14.8%
7D-10.8%
Valor de la cartera
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Citius Pharmaceuticals, Inc.

Informe acción NasdaqCM:CTXR

Capitalización de mercado: US$15.7m

Citius Pharmaceuticals (CTXR) Resumen de Acciones

Citius Pharmaceuticals, Inc. es una empresa biofarmacéutica centrada en el desarrollo y la comercialización de productos para cuidados intensivos. Saber más

Análisis fundamental de CTXR
Puntuación del snowflake
Valoración3/6
Crecimiento futuro5/6
Rendimiento pasado0/6
Salud financiera5/6
Dividendos0/6

Recompensas

Se prevé un crecimiento anual de los beneficios de 55.87%

Cotiza a buen valor en comparación con empresas similares e industria

Análisis de riesgos

Los accionistas han sido diluidos sustancialmente en el último año

Precio de las acciones muy volátil durante los últimos 3 meses en comparación con el mercado US

No tiene una capitalización de mercado significativa ($16M)


CTXR Community Fair Values

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Competidores de Citius Pharmaceuticals, Inc.

Historial de precios y rendimiento

Resumen de las cotizaciones máximas, mínimas y variaciones del Citius Pharmaceuticals
Precios históricos de las acciones
Precio actual de la acciónUS$0.58
Máximo en las últimas 52 semanasUS$2.48
Mínimo de 52 semanasUS$0.48
Beta1.05
Cambio en 1 mes-33.65%
Variación en 3 meses-16.06%
Cambio de 1 año-14.83%
Variación en 3 años-97.91%
Variación en 5 años-98.97%
Variación desde la OPV-99.85%

Noticias y actualizaciones recientes

Recent updates

Artículo de análisis • Apr 06

We Think Citius Pharmaceuticals (NASDAQ:CTXR) Needs To Drive Business Growth Carefully

Even when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...
Artículo de análisis • Dec 08

We're Keeping An Eye On Citius Pharmaceuticals' (NASDAQ:CTXR) Cash Burn Rate

There's no doubt that money can be made by owning shares of unprofitable businesses. For example, although Amazon.com...
Artículo de análisis • Aug 01

Will Citius Pharmaceuticals (NASDAQ:CTXR) Spend Its Cash Wisely?

Even when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...
Artículo de análisis • Apr 12

We Think Citius Pharmaceuticals (NASDAQ:CTXR) Can Afford To Drive Business Growth

Just because a business does not make any money, does not mean that the stock will go down. For example, biotech and...
Artículo de análisis • Dec 25

Here's Why We're Watching Citius Pharmaceuticals' (NASDAQ:CTXR) Cash Burn Situation

Even when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...
Seeking Alpha • Sep 28

Citius Pharma submits biologics license application to FDA for immunotherapy I/ONTAK

Citius Pharmaceuticals (NASDAQ:CTXR) on Wednesday said it had submitted a biologics license application (BLA) to the U.S. FDA for its I/ONTAK immunotherapy for the treatment of cutaneous T-cell lymphoma, a rare type of cancer. According to CTXR, I/ONTAK (denileukin diftitox) is a purified and more bioactive formulation of previously FDA-approved therapy ONTAK. The BLA submission was supported by results from a phase 3 study. The submission comes after CTXR held a pre-BLA meeting with the FDA in July. The company in May had said that it planned to form a new company focused on developing and commercializing I/ONTAK, with an IPO planned for H2 2022. "The BLA filing for denileukin diftitox marks the first of our pipeline candidates to be submitted for FDA approval," CTXR CEO Leonard Mazur said in Wednesday's statement. Citius Pharmaceuticals (CTXR) stock -0.9% to $1.17 in premarket trading.
Seeking Alpha • Aug 11

Citius Pharmaceuticals GAAP EPS of -$0.06

Citius Pharmaceuticals press release (NASDAQ:CTXR): Q3 GAAP EPS of -$0.06. The company has reported $48.0 million in cash and cash equivalents as of June 30, 2022 to support ongoing programs through August 2023
Artículo de análisis • Aug 05

Here's Why Citius Pharmaceuticals (NASDAQ:CTXR) Must Use Its Cash Wisely

We can readily understand why investors are attracted to unprofitable companies. For example, although...
Seeking Alpha • Jul 12

Citius holds pre-biologics license application meeting with FDA for immunotherapy I/ONTAK

Citius Pharmaceuticals (NASDAQ:CTXR) on Tuesday said it had held a pre-biologics license application (BLA) meeting with the U.S. FDA to discuss its I/ONTAK immunotherapy for the treatment of cutaneous T-cell lymphoma, a rare type of cancer. "Based on the FDA's pre-BLA meeting comments, we intend to move forward with our planned BLA submission for I/ONTAK in the second half of 2022," said CTXR CEO Leonard Mazur. The purpose of the pre-BLA meeting was to discuss the content and acceptability of the company's anticipated BLA for I/ONTAK. Citius (CTXR) in May had said that it planned to form a new company focused on developing and commercializing I/ONTAK, with an IPO planned for H2 2022. CTXR stock +1.3% to $0.92 in premarket trading.
Seeking Alpha • Jul 05

Citius Pharmaceuticals: Hoping For A Turnaround Strategy

Citius Pharmaceuticals is yet to release test results a year after it was granted positive recommendation by the Independent Data Monitoring Committee (IDMC) to proceed with the planned trial. With the help of Biorasi, Citius could reach full patient enrolment by the end of 2022, as earlier indicated. Calculations show that Citius' current cash reserves of $55.8 million will only last the company until December 2022, just when it is expected to complete patient enrolment. There is a buy-out possibility after the company announced its intention to spin-off I/Ontak less than a year after license acquisition. Late-stage biopharmaceuticals company Citius Pharmaceuticals, Inc. (CTXR) informed investors that it had selected Biorasi to help it expand its Phase 3 Mino-Lok trial to clinical sites outside the U.S. Well, that formed one of the main highlights of Q2 2022, with investors yet to hear any news about patient enrolment almost 2 months after Biorasi's appointment. Still, there is a lot of excitement among investors with Citius expected to file its biologics license application ((BLA)) for I/ONTAK with the U.S. Food and Drug Administration ((FDA)) later in the second half of 2022. Thesis In this article, I will explain why I am raising my rating of CTXR to hold from sell. The plan to spin off I/Ontak as a standalone company appears to be a strategic move to spearhead growth and attract new investors to the company. As a pure-play oncology-focused biopharmaceutical project, the new company may leverage past mistakes that have delayed the release of topline data for Mino-Lok. Further, new acquisitions are in the offing, especially since the company's finances are inadequate to sustain the company for the next 12 months. Earlier Assessment In my previous article on CTXR, I expressed my concerns over the company's rush to buy E7777 where it burnt a significant amount of cash. Citius is yet to recover, and it is now on the verge of forming a new company to develop and commercialize I/Ontak. This decision comes as no surprise since it had already completed the Phase 3 trial in December 2021. Additionally, the pipeline development for the two main drug candidates: Mino-Lok and E7777 were on different trajectories. Apart from I/Ontak and Mino-Lok, Citius also has in its pipeline Halo-lido, Mino-Wrap, and a Stem cell platform. At the moment, the market is in a bear mode with investors eagerly waiting for some good news within the pipeline development to squeeze the shorts. For Citius, it has been a long time coming. In July 2021, CTXR announced a positive recommendation by the Independent Data Monitoring Committee ((IDMC)) to proceed with the planned Mino-Lok Phase 3 Trial. One year later, the company is yet to release test results. However, with the entry of Biorasi, we expect the company to fast-track patient enrolment. Overview of Patient enrolment and Phase 3 Trial Dynamics The total number of patients planned for Mino-Lok's phase 3 trial is 144, distributed as 1:1 to the standard of care ((SOC)) which is antibiotics. The objective of this trial (as noted in our earlier report) is to evaluate Mino-Lok's efficacy in salvaging colonized central venous catheters in patients with catheter-related or central line-associated bloodstream infection (CRBSI/ CLABSI). This evaluation is compared to the SOC of using antibiotics. In this trial, the protocol will be focused on reaching 92 catheter failure events that also correspond to the 144 patients. Albeit, the company is yet to disclose how many patients it has tested so far and how many events are in the balance. The primary endpoint is the time until catheter failure occurs, expressed in days from randomization into one of the two study arms. Simply put, this means that a patient with a catheter develops a bacterial infection, is subsequently assigned to one of the two study arms, and from then on, the time in days until the catheter needs to be replaced is noted. In the description of the study, this is given as a time frame of 6 weeks. To be able to show the statistical superiority of Mino-Lok over SOC, the time to catheter failure was defined as at least 38 days for Mino-Lok versus 21 days for SOC. The trial started in February 2018 and reached 40% enrollment in September 2019. The next 50% were reached in February 2020 and later 80% were reached in June 2021. This fits pretty nicely to a rate of 2% enrollment per month. It is interesting to note here that the normally increasing speed of enrollment throughout a study due to clinics being added and the slowdown of the study due to the COVID-19 pandemic have balanced each other out. However, there was a fundamental change by Q4 2021. Despite the increasing number of patients during the Covid19 pandemic, the company still expected a prolonged trial that would affect enrolment. This problem necessitated the recruitment of Biorasi. Citius CEO, Myron Holubiak was optimistic about the company's accomplishments in 2022, despite the apparent delays. He stated, As we move into 2022, we anticipate multiple positive milestones. These include accelerated enrollment and completion of the Mino-Lok trial during the year, topline results in the first half of 2022 for the recently completed I/ONTAK (E7777) Pivotal Phase 3 trial followed by a BLA submission in the second half of the year." Before this date, CTXR always said that topline data for Mino-Lok will be published in 2022, suddenly it changed and only completion of the trial (meaning full enrollment) is planned. Right now, there is no further update on the actual state of the enrollment. In February, CTXR again stated that trial completion will be reached in 2022 leaving open the final date for topline data. Enrollment must be higher than 80% but seems to be very slow. CTXR plans to reach full enrollment by the end of 2022. Now, with the help of Biorasi, this could be fastened up. But still, CTXR plans year-end 2022 for full enrollment and as long as we have no further update, we have to calculate with this. Questions are: What happened to the speed of the enrollment in H2 2021? Why was Biorasi asked for help so late? One could have added clinics in other countries also right from the beginning to keep the Phase 3 trial short. I have no idea why they waited so long for this step. Of special note is that the FDA does not require a certain number of patients but wants to see two adequate and well-designed clinical trials. With regards to Mino-Lok, the completed Phase 2 and the ongoing Phase 3 trials will be sufficient. The number of patients per trial strongly depends on the indication, the trial design and the statistical calculations planned and thus are different for every trial. The planned 144 patients in Phase 3 is enough for FDA approval if the results are good, and statistically significant to prove that Mino-Lok is safe. So what is remaining as far as Mino-Lok is concerned? In presenting its phase 3 topline data, Citius will first hold a Pre-NDA (New Drug Application) meeting with the FDA to talk about the NDA filing and if data are enough. It's the first check by FDA if there are enough data. Sometimes FDA demands additional trials, which can be small or even a full Phase 3 trial. Also, check with FDA if any designations will shorten the review process of the FDA from 10 to 6 months. Mino-Lok already was granted fast-track designation by the FDA meaning that their review process will be only 6 months. Writing the NDA application is a time-based process. It must contain all clinical, and pre-clinical data and manufacturing details. It is expected that it will take at least 6 months from filing to submission of data to the FDA (after the release of topline data). After filing the NDA, the FDA takes 2 months to approve or reject the data. After approval, the FDA needs another 6 months (with fast-track designation, otherwise it takes 10 months) to check the NDA and decide about the approval of Mino-Lok. Thus, in general, CTXR has to prepare everything about Mino-Lok including all results and data but also how it is manufactured and the corresponding documents that prove good manufacturing practice and quality control mechanisms, etc. This means that from topline data onward I believe CTXR will need at least 6 months until NDA submission, followed by a total of 8 months (2 months needed by the FDA to accept the filing and 6 months to review the NDA) until the FDA will finally decide if Mino-Lok is approved. This means with topline data in H1 2023, approval could be in mid-2024. Selling Halo-Lido? Investors are looking forward to CTXR's selling of Halo-Lido, especially after the Phase 2B trial. Whether it will be a possibility or not remains a subject under discussion. Still, the company desperately needs financial backup. Before we address the financial standpoint, we need to underscore the fact that the FDA is yet to approve a prescription drug for the treatment of hemorrhoids. Once approved, Halo-Lido could become the first drug to treat hemorrhoids in the US. Citius Chairman, Leonard Mazur confirmed that the company had received several interested buyers back in 2021. We can speculate that one of the buyers may be interested in buying out Citius but may not be interested in I/Ontak or E7777- the reason for the spin-off.
Seeking Alpha • Apr 13

Critical Care Biopharma - Citius Pharmaceuticals

Citius Pharmaceuticals is a late-stage biopharma focused on critical care products. Preventing shareholder dilution. Resumption of clinical trials after COVID-19.
Seeking Alpha • Mar 28

Citius: 2022 Is A Year Of Catalysts

5 Active Programs With Near Term Catalysts. I/ONTEK Topline Data Release Expected As Early As April. Price Target of $10.
Artículo de análisis • Dec 04

We Think Citius Pharmaceuticals (NASDAQ:CTXR) Can Afford To Drive Business Growth

Just because a business does not make any money, does not mean that the stock will go down. For example, biotech and...
Seeking Alpha • Sep 26

Citius Pharmaceuticals, Inc.: Burning Cash Before Commercialization

Citius stock price reacted to no safety concerns identified by the DMC, to surge 102.86% (YoY) and +108.82% (YTD). Citius has prioritized E7777 threatening to derail the company's progression with Mino-Lok. Continual medical development may overthrow the use of CVCs due to the high mortality rate of 12%-25% associated with CLABSI. With a cash balance of $115.7 million, Citius will likely incur a loss in the E7777 transaction. It requires an upfront payment of $40 million and milestone payments of up to $110 million.
Artículo de análisis • Aug 28

Companies Like Citius Pharmaceuticals (NASDAQ:CTXR) Are In A Position To Invest In Growth

There's no doubt that money can be made by owning shares of unprofitable businesses. By way of example, Citius...

Rentabilidad de los accionistas

CTXRUS PharmaceuticalsMercado US
7D-10.8%-0.1%-0.3%
1Y-14.8%38.7%26.7%

Rentabilidad vs. Industria: Los resultados de CTXR fueron inferiores a los de la industria US Pharmaceuticals, que obtuvo un rendimiento del 38.7% el año pasado.

Rentabilidad vs. Mercado: CTXR obtuvo unos resultados inferiores a los del mercado US, que fueron del 26.7% el año pasado.

Volatilidad de los precios

Is CTXR's price volatile compared to industry and market?
CTXR volatility
CTXR Average Weekly Movement18.6%
Pharmaceuticals Industry Average Movement10.0%
Market Average Movement7.2%
10% most volatile stocks in US Market16.2%
10% least volatile stocks in US Market3.2%

Precio estable de las acciones: El precio de las acciones de CTXR ha sido volátil durante los últimos 3 meses en comparación con el mercado US.

Volatilidad a lo largo del tiempo: La volatilidad semanal de CTXR(19%) se ha mantenido estable durante el último año, pero sigue siendo superior al 75% de las acciones de US.

Acerca de la empresa

FundadaEmpleadosCEOPágina web
200723Leonard Mazurcitiuspharma.com

Citius Pharmaceuticals, Inc. es una empresa biofarmacéutica centrada en el desarrollo y la comercialización de productos para cuidados intensivos. Su producto LYMPHIR, aprobado por la FDA, es una inmunoterapia dirigida para el tratamiento del linfoma cutáneo de células T. La cartera de productos en fase avanzada de la empresa incluye Mino-Lok, una solución antibiótica de bloqueo para tratar a pacientes con infecciones del torrente sanguíneo relacionadas con catéteres; Halo-Lido, una formulación tópica de corticosteroides y lidocaína para proporcionar alivio antiinflamatorio y anestésico a personas que padecen hemorroides; y NoveCite, una terapia con células madre mesenquimales para el tratamiento del SDRA. Citius Pharmaceuticals, Inc. se fundó en 2007 y tiene su sede en Cranford, Nueva Jersey.

Resumen de fundamentos de Citius Pharmaceuticals, Inc.

¿Cómo se comparan los beneficios e ingresos de Citius Pharmaceuticals con su capitalización de mercado?
Estadísticas fundamentales de CTXR
Capitalización bursátilUS$15.72m
Beneficios(TTM)-US$46.20m
Ingresos (TTM)US$5.61m
2.8x
Ratio precio-ventas (PS)
-0.3x
Ratio precio-beneficio (PE)

¿Está CTXR sobrevalorada?

Ver valor justo y análisis de valoración

Beneficios e Ingresos

Estadísticas clave de rentabilidad del último informe de resultados (TTM)
Cuenta de resultados (TTM) de CTXR
IngresosUS$5.61m
Coste de los ingresosUS$1.12m
Beneficio brutoUS$4.49m
Otros gastosUS$50.69m
Beneficios-US$46.20m

Últimos beneficios comunicados

Mar 31, 2026

Próxima fecha de beneficios

n/a

Beneficios por acción (BPA)-1.70
Margen bruto80.07%
Margen de beneficio neto-823.34%
Ratio deuda/patrimonio0%

¿Cómo se ha desempeñado CTXR a largo plazo?

Ver rendimiento histórico y comparativa

Análisis de la empresa y estado de los datos financieros

DatosÚltima actualización (huso horario UTC)
Análisis de la empresa2026/05/20 18:11
Precio de las acciones al final del día2026/05/20 00:00
Beneficios2026/03/31
Ingresos anuales2025/09/30

Fuentes de datos

Los datos utilizados en nuestro análisis de empresas proceden de S&P Global Market Intelligence LLC. Los siguientes datos se utilizan en nuestro modelo de análisis para generar este informe. Los datos están normalizados, lo que puede introducir un retraso desde que la fuente está disponible.

PaqueteDatosMarco temporalEjemplo Fuente EE.UU. *
Finanzas de la empresa10 años
  • Cuenta de resultados
  • Estado de tesorería
  • Balance
Estimaciones del consenso de analistas+3 años
  • Previsiones financieras
  • Objetivos de precios de los analistas
Precios de mercado30 años
  • Precios de las acciones
  • Dividendos, escisiones y acciones
Propiedad10 años
  • Accionistas principales
  • Información privilegiada
Gestión10 años
  • Equipo directivo
  • Consejo de Administración
Principales avances10 años
  • Anuncios de empresas

* Ejemplo para valores de EE.UU., para no EE.UU. se utilizan formularios y fuentes normativas equivalentes.

A menos que se especifique lo contrario, todos los datos financieros se basan en un periodo anual, pero se actualizan trimestralmente. Esto se conoce como datos de los últimos doce meses (TTM) o de los últimos doce meses (LTM). Más información.

Modelo de análisis y copo de nieve

Los detalles del modelo de análisis utilizado para generar este informe están disponibles en nuestra página de Github, también tenemos guías sobre cómo utilizar nuestros informes y tutoriales en Youtube.

Conozca al equipo de talla mundial que diseñó y construyó el modelo de análisis Simply Wall St.

Métricas industriales y sectoriales

Simply Wall St calcula cada 6 horas nuestras métricas sectoriales y de sección. Los detalles de nuestro proceso están disponibles en Github.

Fuentes analistas

Citius Pharmaceuticals, Inc. está cubierta por 4 analistas. 2 de esos analistas presentaron las estimaciones de ingresos o ganancias utilizadas como datos para nuestro informe. Las estimaciones de los analistas se actualizan a lo largo del día.

AnalistaInstitución
Jason KolbertD. Boral Capital LLC.
Swayampakula RamakanthH.C. Wainwright & Co.
Jason McCarthyMaxim Group