Tuesday, November 07, 2017 10:04:28 AM
NIA is extremely excited to announce its first ever Biotech Stock Suggestion: Citius Pharmaceuticals, Inc. (CTXR). The company was just listed to the NASDAQ for the first time in August and remains undiscovered at this time. CTXR at $3.76 per share reminds us very much of HIVE trading at $0.74 per share six weeks ago - in terms of having potential to make explosive short-term gains. Less than one week ago, CTXR announced that it received "Fast Track" status from the FDA for its Mino-Lok product and is currently beginning its Phase 3 trials!
Currently, CTXR at $3.76 per share has an extremely low market cap of only $31 million, considering that Mino-Lok is the only product addressing a HUGE unmet market that is estimated to be worth $750 million in the U.S. alone! Central venous catheters (CVCs) are life-saving vascular access ports in patients requiring long-term intravenous therapy. However, of the approximately 7 million CVCs used annually about 500,000 or 7% become infected leading to serious, life-threatening infections known as catheter-related blood stream infections (CRBSIs).
CTXR's Mino-Lok is an antibiotic lock solution used to treat patients with CRBSIs. Currently, the standard of care in the management of CRBSIs consists of removing the infected CVC and replacing it with a new catheter at a different vascular access site. These procedures are costly and 15% to 20% of the procedures are associated with significant morbidity. There are currently no approved therapies to salvage infected CVCs!
Often, the removal of the CVC and reinsertion of a new CVC at a different site may be difficult, or even impossible, because of the unavailability of other accessible vascular sites and the need to maintain infusion therapy. Critically ill patients with short-term catheters often have underlying coagulopathy, where the blood’s ability to clot is impaired. This condition would make reinsertion of a new CVC at a different site risky in terms of mechanical complications.
The FDA only designates Fast Track status to products that treat serious or life-threatening conditions and fill an unmet medical need. It makes Mino-Lok eligible for priority review to shorten the FDA review process from ten months to only six months!
If CTXR receives FDA approval for Mino-Lok, NIA predicts that CTXR will become its next stock to achieve explosive short-term gains similar to the 812.2% rally that HIVE just made! CTXR is located near NIA in NJ and what makes us extremely confident in CTXR's ability to execute is the fact that its Chairman Leonard Mazur recently added 432,400 shares to his position at an average price of $4.09 per share. There is nothing more bullish than the Chairman of a company investing $1.77 million into his own stock to help fund Phase 3 trials!
Take a look at these other biotech stocks that received FDA Fast Track status in recent months:
Pluristem (PSTI) received Fast Track status on September 18, 2017 and the stock rose from $1.23 per share to a high in October of $2.12 per share for a gain of 72.4% in six weeks.
Iovance Biotherapeutics (IOVA) received Fast Track status on August 31, 2017 and the stock rose from $4.50 per share to a high in September of $8.60 per share for a gain of 91.1% in one month.
UroGen Pharma (URGN) received Fast Track status on August 29, 2017 and the stock rose from $18.04 per share to a high yesterday of $38.38 per share for a gain of 112.7% in two months.
CTXR has the lowest market cap out of every biotech stock we are aware of that received Fast Track status from the FDA in 2017!
Recent CTXR News
- Citius Pharmaceuticals Announces Closing of $15 Million Registered Direct Offering • PR Newswire (US) • 04/30/2024 08:05:00 PM
- Citius Pharmaceuticals Announces $15 Million Registered Direct Offering • PR Newswire (US) • 04/26/2024 12:00:00 PM
- Citius Pharmaceuticals Announces Addition of City of Hope to UMN's Phase 1 Trial of LYMPHIR in Combination with CAR-T for the Treatment of B-Cell Lymphoma • PR Newswire (US) • 04/11/2024 12:30:00 PM
- Citius Pharmaceuticals to Present at the LD Micro Invitational XIV Investor Conference • PR Newswire (US) • 04/04/2024 12:30:00 PM
- Citius Pharmaceuticals Announces FDA Acceptance of the BLA Resubmission of LYMPHIR™ (Denileukin Diftitox) for the Treatment of Adults with Relapsed or Refractory Cutaneous T-Cell Lymphoma • PR Newswire (US) • 03/18/2024 12:30:00 PM
- Citius Pharmaceuticals, Inc. Secures $2.4 million through New Jersey Economic Development Program • PR Newswire (US) • 03/07/2024 01:30:00 PM
- Form EFFECT - Notice of Effectiveness • Edgar (US Regulatory) • 03/04/2024 05:15:18 AM
- Citius Pharmaceuticals Announces Filing of Form S-3 Shelf Registration Statement to Replace Expiring Prior Shelf Registration • PR Newswire (US) • 02/26/2024 12:30:00 PM
- Form S-3 - Registration statement under Securities Act of 1933 • Edgar (US Regulatory) • 02/23/2024 09:23:46 PM
- Form S-8 - Securities to be offered to employees in employee benefit plans • Edgar (US Regulatory) • 02/23/2024 09:18:59 PM
- Citius Pharmaceuticals to Participate in Upcoming BIO CEO and Sidoti Investor Conferences • PR Newswire (US) • 02/23/2024 01:30:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 02/15/2024 01:45:11 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 02/14/2024 09:40:26 PM
- Citius Pharmaceuticals, Inc. Reports Fiscal First Quarter 2024 Financial Results and Provides Business Update • PR Newswire (US) • 02/14/2024 09:30:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 02/14/2024 02:18:38 PM
- Citius Pharmaceuticals Resubmits the Biologics License Application of LYMPHIR™ (Denileukin Diftitox) for the Treatment of Adults with Relapsed or Refractory Cutaneous T-Cell Lymphoma • PR Newswire (US) • 02/14/2024 01:01:00 PM
- Form DEFA14A - Additional definitive proxy soliciting materials and Rule 14(a)(12) material • Edgar (US Regulatory) • 01/26/2024 09:08:28 PM
- Form DEF 14A - Other definitive proxy statements • Edgar (US Regulatory) • 01/26/2024 09:05:57 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 01/23/2024 09:05:27 PM
- Citius Pharmaceuticals Announces Nomination of Pharmaceutical Executive Robert J. Smith to its Board of Directors • PR Newswire (US) • 01/23/2024 01:30:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 01/05/2024 09:05:12 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 01/02/2024 09:04:14 PM
- Citius Pharmaceuticals Completes Enrollment in Pivotal Phase 3 Trial of its Mino-Lok® Therapeutic to Salvage Catheters • PR Newswire (US) • 01/02/2024 01:31:00 PM
- Citius Pharmaceuticals, Inc. Reports Fiscal Full Year 2023 Financial Results and Provides Business Update • PR Newswire (US) • 01/02/2024 01:30:00 PM
NanoViricides Reports that the Phase I NV-387 Clinical Trial is Completed Successfully and Data Lock is Expected Soon • NNVC • May 2, 2024 10:07 AM
ILUS Files Form 10-K and Provides Shareholder Update • ILUS • May 2, 2024 8:52 AM
Avant Technologies Names New CEO Following Acquisition of Healthcare Technology and Data Integration Firm • AVAI • May 2, 2024 8:00 AM
Bantec Engaged in a Letter of Intent to Acquire a Small New Jersey Based Manufacturing Company • BANT • May 1, 2024 10:00 AM
Cannabix Technologies to Deliver Breath Logix Alcohol Screening Device to Australia • BLO • Apr 30, 2024 8:53 AM
Hydromer, Inc. Reports Preliminary Unaudited Financial Results for First Quarter 2024 • HYDI • Apr 29, 2024 9:10 AM