Newsletter Subject

Could This Former Nasdaq Breakout Champ (Inside) Be Aiming For A Giant Bounce? Technicals Lean Oversold

From

fierceanalyst.net

Email Address

jaks@fierceanalyst.net

Sent On

Thu, Jul 8, 2021 01:31 PM

Email Preheader Text

Let's get after it because time is of the essence. Could This Former Nasdaq Breakout Champ Be Aiming

Let's get after it because time is of the essence. Could This Former Nasdaq Breakout Champ (CTXR) Be Aiming For A Giant Bounce? Technicals Lean Oversold [Dawson James Securities - $8.00 Price Target]( July 8th, 2021 FierceAnalyst Reader,  Let's get after it because time is of the essence. What I've got for you today is a multi-time past champ. Most recently brought to you back on June 16th, this profile exploded in an epic way. Setting a new 52-week high on June 22nd of $4.56, it leaped approximately 41% and $1.30+ in nearly one week from my early morning alert. Now, here I am again bringing it to you at the opening bell. Why? Well, several potential driver indicators I've highlighted in this report could spark its next major move. Here's why Citius Pharmaceuticals, Inc. (CTXR) needs immediate attention once again... Citius is a late-stage specialty pharmaceutical company dedicated to the development and commercialization of critical care products, with a focus on anti-infectives and cancer care. Now, pay close attention... Citius Pharmaceuticals Is Addressing Several Unmet Needs In The Medical Field Despite current medical advances, there are still many medical conditions with unmet needs. For example, long-term patients with Central Venous Catheters (CVCs) for dialysis or cancer treatment are still at risk for complications related to bloodstream infections that might be fatal. Complications associated with CVC placement can present a 12%-25% morbidity and mortality, resulting in burdening hospitals and healthcare institutions with costs, hospital days, and patient quality of life. Thus, management and prevention should be the ultimate goal for positive treatment outcomes. A company that understands the importance of unmet needs is Citius Pharmaceuticals, Inc. (NASDAQ: CTXR). The company is a specialty pharmaceutical company dedicated to developing and commercializing novel critical care drug products. Citius is currently advancing three proprietary product candidates: Mino-Lok, CITI-002 (Halo Lido) and CITI-101 (Mino-Wrap). They also have therapy for treating ARDS, including ARDS associated with CV-19. This is what you need to know. Citius In The Prevention Of Catheter-Related Bloodstream Infections (CRBSI) And Central Line-Associated Bloodstream Infections (CLABSI) Infected catheters can become fatal, presenting patients with a host of new health problems, especially in cancer patients receiving therapy through central venous catheters (CVCs) and in hemodialysis patients where venous access presents a challenge. Currently, there are no approved therapies to salvage infected CVCs, the standard treatment is removing and replacing (R&R) infected catheters. From the 7,000,000 CVCs used annually in the U.S., up to 472,000 become infected, leading to severe, life-threatening infections called CRBSI/CLABSI. Besides, it is important to acknowledge that hospitals are penalized for reporting high infection rates. The cost to R&R is around $10k. However, if the patients get an infection, the costs and potential patient harm increases significantly. Through Citius novel therapy Mino-Lok solution, catheters can be disinfected and salvaged to prevent the need to replace and restart a deadly and costly process. Additionally, the market opp. for this therapy treatment is estimated at $750Mn per year in the U.S. and is projected to reach $1.84Bn globally in 2028. Clinicians and technologists developed Mino-Lok at M.D. Anderson Cancer Center. Mino-Lok is currently being tested in a Phase 3 trial with the primary endpoint being catheter failures, and it has the potential to change the standard of care for the management of these severe infections. Stem-Cell Therapy For Acute Respiratory Distress Syndrome (ARDS) Another treatment being developed by Citius is stem-cell therapy for acute respiratory distress syndrome (ARDS) under the name Novellus. Matt Angel, Ph.D., CSO of the company, is working with mesenchymal stem cells (MSCs), which have been shown to be safe in over 900 clinical trials and in treating several inflammatory diseases, including ARDS. ARDS is the most common cause of respiratory failure and mortality in CV-19 patients. Its symptoms include shortness of breath, rapid breathing, and bluish skin coloration. For those who survive, a decreased quality of life is common. ------ Now that you have an idea of what's cooking with CTXR, here are its immediate potential driver indicators you need to know this moment: Your No. 1 CTXR Potential Driver Indicator - Oversold Leaning Technicals / Huge Bounce Potential This former champ could be a major bounce candidate in the short term. Here's why. First let's take a look at CTXR's 1-year chart: As you can see, after a June pop to over $4.50, this Nasdaq profile has since been in a downtrend. But, when it dropped to the $2.00 level, it looks like strong potential support could be holding this profile from dropping any further. This could be huge... In the past, this profile has held support at a couple different lines. Back in early March, CTXR dropped to just below $1.50 before climbing back over $2.00. Then, CTXR followed back up with another $1.50 touch in mid-April before climbing back up the charts. Fast-forward to May. After dropping below $2.00 mid-month, it began to heat up towards that 52-week high last month. Now, after this recent downtrend, $2.00 potential support looks to be holding once again which means a bounce could be in the near future. On top of that, [Barchart]( is reporting multiple oversold leaning technicals for CTXR you need to be aware of. They are as follows: - 9-Day Relative Strength Index: 28.39% - 14-Day Relative Strength Index: 36.19% When these numbers drop down to the 30% range and lower, they can be viewed as being in oversold territory. While in this territory, they can paint the picture of a profile that is undervalued. - 14-Day Raw Stochastic: 9.69% - 14-Day Williams %R: 90.31% As the Raw Stochastic nears the 10% range and lower and the Williams %R nears the 90% range or higher, these technical indicators may also be viewed as oversold and undervalued. Could these technicals be signaling a profile that is oversold/undervalued and ready to make another potential vertical move? ----- Your No. 2 CTXR Potential Driver Indicator - Company First Half 2021 Business Update Citius Pharmaceuticals, Inc. Provides First Half 2021 Business Update, Highlights Upcoming Milestones - Phase 3 Mino-Lok® trial proceeding as planned following recommendation by independent Data Monitoring Committee (DMC), highlighting important safety and efficacy signals - - Mino-Lok® New Drug Application (NDA) submission planned for 2022 following anticipated completion of Phase 3 trial by the end of 2021 or early 2022 - - Citius financial flexibility expanded with $127.6Mn in financing activities during the first half of 2021, including $16.9Mn in cash proceeds from warrants exercised during the quarter ended June 30, 2021 - CRANFORD, N.J., July 7, 2021 /PRNewswire/ -- Citius Pharmaceuticals, Inc. ("Citius" or the "Company") (Nasdaq: CTXR), a biopharmaceutical company dedicated to the development and commercialization of first-in-class critical care products with a focus on anti-infective products in adjunct cancer care, unique prescription products and stem cell therapy, today provided a business update for the six-month period ended June 30, 2021 and reported on recent corporate developments. Recent Highlights and Upcoming Milestones - On July 1, 2021, Citius reported that the independent DMC recommended continuation of the Phase 3 Mino-Lok® pivotal superiority trial as planned with no modifications or safety concerns, - Citius expects to complete the Mino-Lok® trial by the end of 2021 or early 2022, subject to continued easing of CV-19 restrictions in the U.S., - Citius plans to submit a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) in 2022 following completion of its Phase 3 Mino-Lok® trial, and - Subsequent to March 31, 2021, Citius issued 11.2 million shares of Citius common stock upon the exercise of warrants, for aggregate proceeds of $16.9Mn during the quarter and a total of $127.6Mn in financing activities during the first half of 2021. "On July 1, 2021, we reported that the independent Data Monitoring Committee (DMC), following its third interim review, recommended continuing the Phase 3 trial for Mino-Lok® without modification. This recommendation affirms that there is an important efficacy signal that merits moving forward with the trial, there are no safety concerns to warrant halting the trial, and that the full data set upon trial completion may support statistically significant superiority. Whether Mino-Lok® demonstrates statistical superiority will only be known to us once the trial is finished and the data is unblinded. We view the recommendation of the DMC as a strong positive signal, and remain fully committed to completing the trial in a timely manner," stated Myron Holubiak, President and Chief Executive Officer of Citius. [...] [Read the full article here.]( ----- Your No. 3 CTXR Potential Driver Indicator - Company Being Added To Russell 2000® Index Citius Pharmaceuticals to be Added to Russell 2000® Index CRANFORD, N.J., June 7, 2021 /PRNewswire/ -- Citius Pharmaceuticals, Inc. ("Citius" or the "Company") (Nasdaq: CTXR), a biopharmaceutical company dedicated to the development and commercialization of first-in-class critical care products with a focus on anti-infective products in adjunct cancer care, unique prescription products and stem cell therapy, today announced that it is set to be added to the Russell 2000® Index at the conclusion of the Russell US Indexes annual reconstitution, effective at the opening of the U.S. equity markets on June 28, 2021. "Our inclusion in the Russell index is an important milestone for Citius that reflects the continued progress we are making to develop and commercialize first-in-class treatment options for patients around the world. We welcome the enhanced visibility of our diversified pipeline and long-term growth potential, and look forward to sharing our future milestones with a broader investment community," said Myron Holubiak, President and Chief Executive Officer of Citius. FTSE Russell determines membership for its Russell indexes primarily by objective, market-capitalization rankings and style attributes. Membership in the small-cap Russell 2000® Index, which remains in place for one year, is based on membership in the broad-market Russell 3000® Index. Citius st-ock will also be automatically added to the appropriate growth and value indexes. Russell indexes are widely used by investment managers and institutional investors for index funds and as benchmarks for active investment strategies. Approximately $9Tn in assets are benchmarked against Russell's US indexes. Russell indexes are part of FTSE Russell, a leading global index provider. [Read the full article here.]( ----- Your No. 4 CTXR Potential Driver Indicator - Analyst Coverage With Major P.T. [Dawson James Securities - $8.00 Price Target]( Here are the major highlights from the March Dawson James Securities updated analyst report: Management is Focused and Understands. Now is the time to spend money on resources, FDA consultants and the like to ensure that all elements of the rolling NDA are up to par, from the culmination of component studies to CMC details, record keeping and, of course, a focus on the potential for the pivotal trial to be stopped early for efficacy. What is Mino-Lok? Three active drug substances (minocycline, ethanol, and EDTA), which are combined into two vials, MLT01 (minocycline) and MLT02 (ethanol and EDTA). Citius has manufactured three registration lots of Mino-Lok using the commercial manufacturing process, part of the planned New Drug Application (NDA). Citius has placed all registration lots on stability at the appropriate ICH (The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use) conditions to support the NDA filing. Citius has also developed a new exclusive synthesis process for disodium edetate, a chelating agent that supplants heparin as the anti-clotting agent in Mino-Lok. Trial Background. The current Phase 3 trial being conducted compares Mino-Lok therapy (MLT) to the standard of care, which is antibiotic lock therapy (ALT). This is used to disinfect colonized catheters causing bacteremia and keep the treated catheters functioning and infection-free for eight weeks post-therapy. The current primary endpoint in the study is planned to demonstrate a significant difference in the time to catheter failure when comparing MLT to ALT. This is clinically important because eliminating the source of infection enables antibiotic treatment of the bacteremia to work more effectively and expeditiously. Additionally, if a catheter can be maintained for the time that it is needed, the patient does not need to be subjected to the procedures for removing and replacing the catheters that are associated with some serious adverse events. Could the DMC halt the study early for Efficacy? We think so. This past September, the DMC recommended continuing the trial without any modifications. The DMC further requested to have an ad hoc meeting in the near future. Recall that the trial (Sept. 2019) reached the first interim analysis point of 37 catheter failures representing 40% of the anticipated events at ~58 patients. Recall that the trial is designed with 80% power for an assumed 17-day difference between active and standard of care (SOC). We typically expect the SOC arm to fail in 5-14 days. Valuation. Our valuation is based on our therapeutic models and associated assumptions projected to 2028. The lead product, MiniLok, is now in a Phase 3 trial. We conservatively assume just 50% probability of success in our therapeutic model. On top of this, we also use a 30% risk rate in our free cash flow to the firm (FCFF), our discounted EPS (dEPS) and sum-of-the-parts (SOP) models. We equal weight and average these metrics and then round to the nearest whole number to derive our $8.00 price target. ----- From Wednesday's close, this $8.00 price target provides upside potential over 200%. Now, I'm not saying CTXR is going to go soaring to $8.00 today, but you need to be aware of this analyst provided potential upside. ----- Your No. 5 CTXR Potential Driver Indicator - Bullish Technicals According to [Barchart]( at close Wednesday, CTXR is packing some seriously bullish technical indicators. These are currently triggered as bullish: Short Term Indicators - 20 - 50 Day MACD Oscillator - 20 - 100 Day MACD Oscillator - 20 - 200 Day MACD Oscillator Medium Term Indicators - 50 - 100 Day MACD Oscillator - 50 - 150 Day MACD Oscillator - 50 - 200 Day MACD Oscillator Long Term Indicators - 150 Day Moving Average - 200 Day Moving Average - 100 - 200 Day MACD Oscillator Even after this recent downtrend from CTXR, could these bullish technicals be telling a different story of things to come for this Nasdaq past champ? ----- Recap: Top 5 Potential CTXR Driver Indicators #1. Oversold Leaning Technicals / Huge Bounce Potential #2. Company First Half 2021 Business Update #3. Company Being Added To Russell 2000® Index #4. Analyst Coverage With Major P.T. #5. Bullish Technicals ----- Coverage is officially reinitiated on CTXR. Also, when you have a moment later on, do this: If there are any updates today, I'll get them out to you quickly. Sincerely, Fierce Analyst | Jaks Swift Editorial Writer [Source]( Fierce | 539 W Commerce St, Dallas, TX 75208 [Unsubscribe {EMAIL}]( [Update Profile]( | [Constant Contact Data Notice]( Sent by jaks@fierceanalyst.net

EDM Keywords (192)

world working work welcome wednesday warrants viewed view valuation used us understands unblinded trial towards total top today time think things therapy tested territory telling technicals take survive support sum success subsequent submit subjected study still standard stability source since signaling shown sharing set see salvaged safe russell round risk restart requested reported replacing replace removing remains reflects recommendation ready quarter projected profile procedures prevention prevent present potential planned placed place picture pharmaceuticals penalized patient past part par paint packing oversold opening needed need mortality moment modifications might metrics membership means may management making maintained lower look like life known know keep infection inclusion important importance idea huge host hospitals holding highlighted higher heat harmonisation got going get food focused focus first finished fail exercise estimated essence ensure end eliminating elements efficacy effectively edta dropping dropped downtrend dmc disinfected dialysis development developing developed develop designed derive demonstrate deadly data currently culmination ctxr cso course could costs cost cooking conclusion completing complete company common commercialization come combined close citius change catheters catheter care bringing benchmarks benchmarked began based barchart bacteremia back aware average associated assets alt also aiming added active acknowledge 2028 2021 200

Marketing emails from fierceanalyst.net

View More
Sent On

05/12/2024

Sent On

04/12/2024

Sent On

04/12/2024

Sent On

26/11/2024

Sent On

26/11/2024

Sent On

26/11/2024

Email Content Statistics

Subscribe Now

Subject Line Length

Data shows that subject lines with 6 to 10 words generated 21 percent higher open rate.

Subscribe Now

Average in this category

Subscribe Now

Number of Words

The more words in the content, the more time the user will need to spend reading. Get straight to the point with catchy short phrases and interesting photos and graphics.

Subscribe Now

Average in this category

Subscribe Now

Number of Images

More images or large images might cause the email to load slower. Aim for a balance of words and images.

Subscribe Now

Average in this category

Subscribe Now

Time to Read

Longer reading time requires more attention and patience from users. Aim for short phrases and catchy keywords.

Subscribe Now

Average in this category

Subscribe Now

Predicted open rate

Subscribe Now

Spam Score

Spam score is determined by a large number of checks performed on the content of the email. For the best delivery results, it is advised to lower your spam score as much as possible.

Subscribe Now

Flesch reading score

Flesch reading score measures how complex a text is. The lower the score, the more difficult the text is to read. The Flesch readability score uses the average length of your sentences (measured by the number of words) and the average number of syllables per word in an equation to calculate the reading ease. Text with a very high Flesch reading ease score (about 100) is straightforward and easy to read, with short sentences and no words of more than two syllables. Usually, a reading ease score of 60-70 is considered acceptable/normal for web copy.

Subscribe Now

Technologies

What powers this email? Every email we receive is parsed to determine the sending ESP and any additional email technologies used.

Subscribe Now

Email Size (not include images)

Font Used

No. Font Name
Subscribe Now

Copyright © 2019–2025 SimilarMail.