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Chimerix, Inc.NasdaqGM:CMRX Rapporto sulle azioni

Cap. di mercato US$801.1m
Prezzo delle azioni
n/a
US$8.53
n/dsconto intrinseco
1Y822.9%
7D-0.1%
1D
Valore del portafoglio
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Chimerix, Inc.

Report azionario NasdaqGM:CMRX

Capitalizzazione di mercato: US$801.1m

This company has been acquired

The company may no longer be operating, as it has been acquired. Find out why through their latest events.

Chimerix (CMRX) Panoramica del titolo

Chimerix, Inc. è un'azienda biofarmaceutica che sviluppa farmaci per migliorare e prolungare la vita dei pazienti affetti da malattie mortali negli Stati Uniti. Maggiori dettagli

CMRX analisi fondamentale
Punteggio fiocco di neve
Valutazione0/6
Crescita futura2/6
Prestazioni passate0/6
Salute finanziaria6/6
Dividendi0/6

Premi

Si prevede che i ricavi cresceranno 56.38% all'anno

Analisi del rischio

Realizza un fatturato inferiore a 1 milione di dollari ( $212K )

Prezzo delle azioni altamente volatile negli ultimi 3 mesi rispetto al mercato US

Attualmente non redditizio e non si prevede che diventerà redditizio nei prossimi 3 anni


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Concorrenti di Chimerix, Inc.

Storia dei prezzi e prestazioni

Riepilogo dei massimi, dei minimi e delle variazioni dei prezzi delle azioni per Chimerix
Prezzi storici delle azioni
Prezzo attuale dell'azioneUS$8.54
Massimo di 52 settimaneUS$8.55
Minimo di 52 settimaneUS$0.75
Beta-0.18
Variazione di 1 mese0.47%
Variazione a 3 mesi125.93%
Variazione di 1 anno822.94%
Variazione a 3 anni81.32%
Variazione a 5 anni465.56%
Variazione dall'IPO-54.55%

Notizie e aggiornamenti recenti

Seeking Alpha • Feb 20

Chimerix: Potential 'First' In Targeting Recurrent High-Grade Glioma Patients

Summary The company holds the potential to have the first approval of dordaviprone for the treatment of recurrent H3 K27M mutant high-grade glioma patients; PDUFA with a Priority Review date of August 18th, 2025. The global brain tumor therapeutics market is expected to grow to $5.28 billion by 2030; the Company notes that it could obtain >$1 billion in revenues in the United States alone. Phase 3 ACTION study using dordaviprone for the treatment of front-line H3 K27M mutant high-grade glioma patients to have OS interim data readout in Q3 of 2025. FDA approval of dordaviprone for the treatment of patients with recurrent H3 K27M mutant high-grade glioma could allow the company to receive a Priority Review Voucher, which it could keep or sell. Read the full article on Seeking Alpha
Seeking Alpha • Dec 11

Chimerix: Big News, Big Moves, So Maybe Now's The Time To Buy

Summary Chimerix, Inc.'s dordaviprone shows promise in treating H3 K27M-positive glioma, with a potential FDA approval and commercial launch by Q3 2025. CMRX's strong clinical data and high unmet need in diffuse midline glioma bolster confidence in FDA approval, despite potential timeline uncertainties. Financially, CMRX has a cash runway of 6–7 quarters, sufficient to reach an FDA decision, but risks of dilution remain. Given the recent market surge and promising outlook, I maintain a favorable rating on CMRX stock, anticipating significant market capitalization growth. Read the full article on Seeking Alpha

Recent updates

Seeking Alpha • Feb 20

Chimerix: Potential 'First' In Targeting Recurrent High-Grade Glioma Patients

Summary The company holds the potential to have the first approval of dordaviprone for the treatment of recurrent H3 K27M mutant high-grade glioma patients; PDUFA with a Priority Review date of August 18th, 2025. The global brain tumor therapeutics market is expected to grow to $5.28 billion by 2030; the Company notes that it could obtain >$1 billion in revenues in the United States alone. Phase 3 ACTION study using dordaviprone for the treatment of front-line H3 K27M mutant high-grade glioma patients to have OS interim data readout in Q3 of 2025. FDA approval of dordaviprone for the treatment of patients with recurrent H3 K27M mutant high-grade glioma could allow the company to receive a Priority Review Voucher, which it could keep or sell. Read the full article on Seeking Alpha
Seeking Alpha • Dec 11

Chimerix: Big News, Big Moves, So Maybe Now's The Time To Buy

Summary Chimerix, Inc.'s dordaviprone shows promise in treating H3 K27M-positive glioma, with a potential FDA approval and commercial launch by Q3 2025. CMRX's strong clinical data and high unmet need in diffuse midline glioma bolster confidence in FDA approval, despite potential timeline uncertainties. Financially, CMRX has a cash runway of 6–7 quarters, sufficient to reach an FDA decision, but risks of dilution remain. Given the recent market surge and promising outlook, I maintain a favorable rating on CMRX stock, anticipating significant market capitalization growth. Read the full article on Seeking Alpha
Articolo di analisi • Jul 16

We're Keeping An Eye On Chimerix's (NASDAQ:CMRX) Cash Burn Rate

We can readily understand why investors are attracted to unprofitable companies. For example, biotech and mining...
Seeking Alpha • Aug 23

Chimerix: Advancement For Rare Brain Cancer Drug Targeting Specific Mutation

Initiation of phase 3 ACTION study using ONC201 for treatment of glioma patients who harbor the H3 K27M mutation is expected in the 2nd half of 2022. Interim results from the ACTION study are expected in early 2025, with final results expected in 2026. Proof of concept data using ONC201 has already been established in two phase 2 studies; in patients with H3 K27M mutation gliomas and neuroendocrine tumors. Additional imipridones being developed in the pipeline are ONC206 and ONC212 for oncology indications; CMX521 being advanced as prophylactic and treatment for Covid-19. Chimerix, Inc. (CMRX) is a great speculative biotech that should be on your radar. While it is still a risky longer-term play, I believe it could have value based on established proof of concept using ONC201 for the treatment of patients with H3 K27M-mutant glioma. In a phase 2 study, it showed to improve overall survival rates in this specific population, which I will show below. The only downside is that the first interim analysis is not expected until early 2025 with final data not coming out until 2026. However, ONC201 is also being explored in a phase 2 study in neuroendocrine tumors. Such neuroendocrine tumors being explored are Pheochromocytoma/paraganglioma. Initial data was revealed which established some proof of concept of the mechanism of action. Even then, it is working on a second generation imipridone known as ONC206 which is much improved compared to 1st generation ONC201. It is believed that ONC206 provides greater anti-tumor activity compared to ONC201 and thus it is also being advanced in the pipeline. The biotech also entered into an agreement with Emergent BioSolutions ((EBS)) for the sale of worldwide rights to TEMBEXA for a $225 million upfront payment, potential milestone payments and double-digit royalties on net sales as well. It is important to note that this agreement is still in the process of being completed. This agreement relies on additional items being executed. If the agreement goes through with EBS, then the biotech will have enough cash into 2027. Lastly, it is in the process of developing an improved oral formulation of CMX521 as a prophylactic and treatment of SARS-CoV-2 (Covid-19) in collaboration with the Rapidly Emerging Antiviral Drug Development Initiative ((READDI)). While early in the process and already many approved treatments in this space, I believe it could still act as a catalyst if it is successfully advanced. It is believed that animal data will be released in the 2nd half of 2022 on such an improved oral formulation for CMX521 for Covid-19. With a growing pipeline, plus some established proof of concept of ONC201 in a rare brain glioma and neuroendocrine tumors, I believe it is a great speculative biotech play to look into. Imipridone ONC201 Could Possibly Greatly Improve Overall Survival Rates For Rare Gliomas The main drug in Chimerix's pipeline would be ONC201, which is being developed for the treatment of patients with gliomas who harbor the H3 K27M mutation. What occurs with respect to this specific type of glioma? What occurs is the H3K27M mutation itself puts in a new amino acid known as H3, which promotes a gene expression that enable tumor growth to occur. Patients with this type of glioma have poor prognosis and definitely need new types of treatments to be approved. Before diving into ONC201 clinical results, it's important to understand what the drug actually is. Again, it is an imipridone which targets G protein-coupled receptors (GPCRs) and mitochondrial caseinolytic protease p (ClpP), resulting in cancer death. Cell death happens with the induction of the integrated stress response and upregulation pathway of apoptotic (cell death) factors, such as tumor necrosis factor ((TNF)) related apoptosis-inducing ligand ((TRAIL)). More specifically, it selectively induces cell death by binding and altering activity of DRD2 (Selectively coupled G-protein receptor) and ClpP. This is further established with the following action: DRD2 antagonism is responsible for inhibiting Ras signaling pathway that cancer has ClpP degrades excess amount of mitochondrial proteins which are important for the cancer cell to be viable Remember above when I stated that H3 K27M mutation uses amino acid H3 to promote gene expression for the cancer? Well, ONC201 was established to alter this gene expression making it sensitive to the drug itself. All these actions are what are put in place to specifically treat glioma patients who harbor the H3 K27M mutation. Moving onto the program advancement at hand, the company intends to initiate a phase 3 study in the 2nd half of 2022 known as ACTION. This is going to be a randomized late-stage study using ONC201 for the treatment of newly diagnosed diffuse glioma patients whose tumors harbor the H3 K27M mutation. It is expected that about 450 patients will be randomized 1:1:1 to receive doses as followed: 625 mg ONC201 once per week 625 mg ONC201 twice per week Placebo The primary endpoint of this study is overall survival ((OS)). Patients will first be treated with radiation and then be randomized to one of the dosing groups noted directly above. As far as catalysts go for this study, it could be quite some time to see data. It is said that the first interim analysis for results is not expected until 2025. From there, final data from this ACTION study is not expected until 2026. The thing is that it may be a good market to tap into despite the fact how rare the H3 K27M mutation glioma is. Chimerix believes it can earn above $500 million in sales annually should it ultimately get ONC201 to market for this specific population. Despite results taking time to come out, it's important to note that there is a great shot at clinical success. That's because ONC201 monotherapy was able to achieve an overall response rate ((ORR)) of 30% by RANO HGG and/or LGG by dual reader BICR. Even better, is what those treated with this drug obtained in terms of overall survival rates. For the H3 K27M recurrent glioma patients given ONC201, overall survival at 12 months and 24 months was 57% and 35%, respectively, whereas historical control at 12 months and 24 months was 27.5% and 6.4%, respectively. What does this show? This shows that with the biotech specifically targeting patients with this H3 K27M mutation by using ONC201, it can improve overall survival for them. Proof Of Concept For ONC201 In Treatment Of Patients With Neuroendocrine Tumors In addition to some proof of concept being established in a phase 2 study with ONC201 in patients with H3 K27M mutated gliomas, the drug had also seen some mechanism of action in patients with neuroendocrine tumors. One neuroendocrine tumor being explored is paraganglioma. A paraganglioma is a type of neuroendocrine tumor that forms near certain blood vessels and nerves outside of the adrenal glands. The adrenal glands being affects is not a very good thing, considering they are responsible for making hormones which control many functions in the body. In an open-label phase 2 investigator-initiated study with 30 patients, treatment with ONC201 performed pretty well. The cohort of paraganglioma patients who were dosed with ONC201 once a week performed better than the other cohort of patients dosed twice a week with ONC201. For these patients who were dosed once weekly with ONC201, the outcome was as follows: 5 out of 10 patients (50%) achieved a partial response ((PR)) 2 out of 10 patients achieved stable disease ((SD)) The other neuroendocrine tumor also being evaluated with the use of this drug is Pheochromocytoma, which is a hormone secreting tumor that can occur in the adrenal glands. Additional Shots On Goal With Imipridones ONC206 And ONC212
Articolo di analisi • Jul 20

Here's Why We're Watching Chimerix's (NASDAQ:CMRX) Cash Burn Situation

Just because a business does not make any money, does not mean that the stock will go down. For example, although...
Seeking Alpha • Jun 06

Chimerix: Down But Not Out

Today, we revisit an interesting small-cap concern called Chimerix that trades for around two bucks a share, and under cash value. The company recently announced a deal to sell off its one approved drug for over $200 million, which was received negatively by the market. Chimerix will now pivot fully to developing the other parts of its pipeline. We revisit the investment case around Chimerix in the paragraphs below.
Seeking Alpha • Jan 05

Chimerix: Searching For Clarity

Today, we put Chimerix, Inc. in the spotlight for the first time. The company recently received an FDA approval and has several other promising compounds in development. A full investment analysis is provided in the paragraphs below.
Articolo di analisi • Dec 24

Does Chimerix (NASDAQ:CMRX) Have A Healthy Balance Sheet?

The external fund manager backed by Berkshire Hathaway's Charlie Munger, Li Lu, makes no bones about it when he says...
Articolo di analisi • Sep 16

Is Chimerix (NASDAQ:CMRX) A Risky Investment?

Howard Marks put it nicely when he said that, rather than worrying about share price volatility, 'The possibility of...
Articolo di analisi • Jun 08

Does Chimerix (NASDAQ:CMRX) Have A Healthy Balance Sheet?

David Iben put it well when he said, 'Volatility is not a risk we care about. What we care about is avoiding the...
Articolo di analisi • May 13

Chimerix, Inc. (NASDAQ:CMRX): Are Analysts Optimistic?

With the business potentially at an important milestone, we thought we'd take a closer look at Chimerix, Inc.'s...

Rendimenti per gli azionisti

CMRXUS BiotechsUS Mercato
7D-0.1%-1.6%-0.8%
1Y822.9%34.4%27.1%

Ritorno vs Industria: CMRX ha superato il US Biotechs che ha restituito 34.4 % nell'ultimo anno.

Rendimento vs Mercato: CMRX ha superato il mercato US che ha restituito 27.1 % nell'ultimo anno.

Volatilità dei prezzi

Is CMRX's price volatile compared to industry and market?
CMRX volatility
CMRX Average Weekly Movement21.2%
Biotechs Industry Average Movement11.0%
Market Average Movement7.2%
10% most volatile stocks in US Market16.3%
10% least volatile stocks in US Market3.2%

Prezzo delle azioni stabile: Negli ultimi 3 mesi il prezzo delle azioni di CMRX è stato volatile rispetto al mercato US.

Volatilità nel tempo: La volatilità settimanale di CMRX è diminuita da 34% a 21% nell'ultimo anno, ma è comunque superiore al 75% delle azioni US.

Informazioni sull'azienda

FondatoI dipendentiAMMINISTRATORE DELEGATOSito web
200079Mike Andriolewww.chimerix.com

Chimerix, Inc. è una società biofarmaceutica che sviluppa farmaci per migliorare e prolungare la vita dei pazienti affetti da malattie mortali negli Stati Uniti. La sua pipeline di prodotti comprende il dordaviprone (ONC201), in fase di sviluppo clinico 3 per il glioma diffuso H3 K27M-mutante e in fase 2 di sperimentazione clinica avviata dagli sperimentatori per diversi studi oncologici, e ONC206, un agonista ClpP di seconda generazione a base di imipridone e antagonista DRD2, in fase 1 di sperimentazione clinica per il trattamento del sistema nervoso centrale e di altri tumori solidi. L'azienda sviluppa anche ONC212, un imipridone, agonista sperimentale del soppressore tumorale GPCR orfano GPR132 e del ClpP, in fase di sperimentazione preclinica, e CMX521, un analogo nucleosidico candidato a farmaco antivirale per il trattamento di nuovi coronavirus.

Chimerix, Inc. Riepilogo dei fondamenti

Come si confrontano gli utili e i ricavi di Chimerix con la sua capitalizzazione di mercato?
CMRX statistiche fondamentali
Capitalizzazione di mercatoUS$801.08m
Utili (TTM)-US$88.39m
Ricavi(TTM)US$212.00k
3,779x
Rapporto P/S
-9.1x
Rapporto P/E

CMRX è sopravvalutato?

Vedi Fair Value e analisi di valutazione

Utili e ricavi

Statistiche chiave sulla redditività dall'ultima relazione sugli utili (TTM)
CMRX Conto economico (TTM)
RicaviUS$212.00k
Costo del fatturatoUS$74.57m
Profitto lordo-US$74.36m
Altre speseUS$14.03m
Utili-US$88.39m

Ultimi utili riportati

Dec 31, 2024

Prossima data di guadagno

n/a

Utile per azione (EPS)-0.94
Margine lordo-35,076.42%
Margine di profitto netto-41,691.98%
Rapporto debito/patrimonio netto0%

Come si è comportato CMRX nel lungo periodo?

Vedi performance storica e confronto

Analisi aziendale e situazione dei dati finanziari

DatiUltimo aggiornamento (ora UTC)
Analisi dell'azienda2025/04/22 01:50
Prezzo dell'azione a fine giornata2025/04/17 00:00
Utili2024/12/31
Utili annuali2024/12/31

Fonti dei dati

I dati utilizzati nella nostra analisi aziendale provengono da S&P Global Market Intelligence LLC. I seguenti dati sono utilizzati nel nostro modello di analisi per generare questo report. I dati sono normalizzati, il che può comportare un ritardo nella disponibilità della fonte.

PacchettoDatiTempisticaEsempio Fonte USA *
Dati finanziari della società10 anni
  • Conto economico
  • Rendiconto finanziario
  • Bilancio
Stime di consenso degli analisti+3 anni
  • Previsioni finanziarie
  • Obiettivi di prezzo degli analisti
Prezzi di mercato30 anni
  • Prezzi delle azioni
  • Dividendi, scissioni e azioni
Proprietà10 anni
  • Top azionisti
  • Insider trading
Gestione10 anni
  • Team di leadership
  • Consiglio di amministrazione
Sviluppi principali10 anni
  • Annunci aziendali

* Esempio per i titoli statunitensi, per i titoli non statunitensi si utilizzano forme e fonti normative equivalenti.

Se non specificato, tutti i dati finanziari si basano su un periodo annuale ma vengono aggiornati trimestralmente. Si tratta dei cosiddetti dati TTM (Trailing Twelve Month) o LTM (Last Twelve Month). Per saperne di più.

Modello di analisi e Snowflake

I dettagli del modello di analisi utilizzato per generare questo report sono disponibili sulla nostra pagina Github; abbiamo anche guide su come utilizzare i nostri report e tutorial su Youtube.

Scoprite il team di livello mondiale che ha progettato e realizzato il modello di analisi Simply Wall St.

Metriche di settore e industriali

Le nostre metriche di settore e di sezione sono calcolate ogni 6 ore da Simply Wall St; i dettagli del nostro processo sono disponibili su Github.

Fonti analitiche

Chimerix, Inc. è coperta da 15 analisti. 2 di questi analisti ha fornito le stime di fatturato o di utile utilizzate come input per il nostro report. Le stime degli analisti vengono aggiornate nel corso della giornata.

AnalistaIstituzione
Geoffrey MeachamBarclays
Debjit ChattopadhyayBrean Capital Historical (Janney Montgomery)
Ritu BaralCanaccord Genuity