(Nasdaq: MDCX) Comes Out Making Early Green Moves (Low Float Idea With Strong Analyst Targets)

*Disseminated on behalf of Medicus Pharma Ltd.


(Nasdaq: MDCX) Comes Out Making Early Green Moves (Low Float Idea With Strong Analyst Targets)



October 20th

Greetings Readers,


Medicus Pharma Ltd. (Nasdaq: MDCX) is taking the the top spot on Monday's watchlist.


Here's why...


Going green early, it's key to take note of MDCX's explosive analyst targets.


At this moment, MDCX may have an approx. 800+% potential upside from current levels (as of writing) to a MarketBeat reported average analyst target of $23.50.


Furthermore, a float of fewer than 5Mn shares needs to be acknowledge as volatility potential could be significantly heightened.


And remember, MDCX is not too far out from a game-changing acquisition being completed.


Spend a second to review the (Nasdaq: MDCX) report below and consider this profile for your radar.

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Across the fast-changing world of life sciences, a few companies are standing out for developing therapies that tackle serious, unmet health needs.


One company, operating through its wholly owned subsidiary, is testing a dissolvable microneedle patch that delivers chemotherapy straight into tumors—an innovation aimed at reshaping treatment for skin cancers like basal cell carcinoma.


Now in clinical trials in the U.S. and the United Arab Emirates, this method could offer a less invasive, more patient-friendly alternative to surgery or systemic chemotherapy.


The company is also growing through targeted acquisitions, including a UK-based biotech focused on advanced prostate disease.


These moves reflect a broader mission to improve care in areas where safer, more effective treatments remain limited.


By combining research-driven development with strong industry ties, the organization aims to bring new therapies to market quickly. In a booming biotech landscape, its efforts stand out for setting fresh benchmarks in both human and veterinary medicine.


And with a float of fewer than 5Mn, a freshly completed acquisition hot off the press, and multiple analyst targets suggesting massive upside potential, this Nasdaq profile has just overtaken my watchlist once again.


What's that? Oh, yeah! This profile was previously alerted only to watch it move approximately 45% from an August 18th open of $2.10 to a recent $3.05 high towards the end of last month.


Take a moment to consider this idea for your radar:


*Medicus Pharma Ltd. (Nasdaq: MDCX)*


Medicus Pharma Ltd. is a biotech/life sciences company focused on accelerating the clinical development programs of novel and disruptive therapeutics assets. The company is actively engaged in multiple countries, spread over three continents.


And based on several potential catalysts, (Nasdaq: MDCX) has pushed its way to the top of my watchlist. Take a look:


No. 1 - A Low Float Could Create The Environment For Heightened Volatility.


No. 2 - A Game-Changing Acquisition Gets Completed!


No. 3 - An Average Of 6 Analyst Targets Suggest Major Upside Potential (Triple-Digit!).


No. 4 - Confidence Increases As Commercial Viability Could Come Into Focus In 2027.


No. 5 - A Significant Update Shares Progression In Key Phase 2 Clinical Study.


But more on those in a second...


Company Breakdown - Medicus Pharma Ltd. (Nasdaq: MDCX)


Medicus Pharma Ltd. specializes in rapidly moving forward the clinical development of cutting-edge therapeutic solutions within the biotech and life sciences sector.

About SkinJect - Medicus Pharma's (Nasdaq: MDCX) Wholly Owned Subsidiary


A novel non-invasive regimen to treat skin cancer; especially Basal Cell Carcinoma.


SkinJect Inc. is a development stage biotechnology life sciences company focused on commercializing novel treatment for non-melanoma skin cancer, especially basal cell carcinoma, using a patented dissolvable doxorubicincontaining microneedle arrays (D-MNA). D-MNA delivers the chemotherapeutic agent transdermally at the site of the lesion to eradicate tumor cells. The relevant US Patents were granted to University of Pittsburgh and Carnegie Mellon University in 2018.

SkinJect Inc. secured exclusive worldwide development and commercialization rights from University of Pittsburgh and Carnegie Mellon University in April 2016. The company attempts to provide an alternative to an invasive, painful, but effective treatment commonly called Mohs Surgery, by providing an efficacious, painless and easy to administer treatment in an office setting.


SkinJect Inc. has completed a Phase I study in March 2021 for participants with superficial and nodular Basal Cell Carcinoma (BCC). In January 2024 a Phase 2 IND clinical protocol was submitted to the FDA for a randomized, controlled, double-blind, multicenter study that is expected to randomize up to 60 patients. Patient recruitment began in August 2024 in 9 sites across the United States. A positively trending interim analysis in March 2025 showed more than 60% complete clinical response. In April 2025, IRB approved an increase in the number of patients from 60 to 90.


SkinJect Clinical Development Outlook

The SkinJect Value Proposition


1. Innovative Microneedle Patch Technology:


  • The company aims to provide an alternative to an invasive, painful, but effective treatment commonly called Mohs Surgery, by providing an efficacious, painless and easy to administer treatment in an office setting.
  • Patented technology for non-invasively treating skin cancer using cellulose-based microneedles to deliver cancer drugs directly to the tumor site
  • Exclusive worldwide development and commercialization rights from University of Pittsburgh and Carnegie Mellon University in April 2016.


2. Market Potential:


  • BCC is the most common and fastest-growing cancer globally.
  • >US$15Bn market for skin cancer treatments in North America by 2030. (1)
  • Potential for further market expansion and penetration by SkinJect’s novel treatment approach.


3. Positive Clinical Trial Results:


  • Phase 1 trial completed March 2021, demonstrating safety and tolerability.
  • In Q1 2024 a Phase 2 IND clinical protocol was submitted to the FDA for a randomized, controlled, double-blind, multicenter study.
  • In Q3 2024 Phase 2 enrollment began.
  • In Q1 2025 conducted interim analysis after 50% patient recruitment.
  • In Q2 2025, IRB approved to increase number of patients from 60 to 90.


4. Seasoned Leadership and Board:


  • Management team with public company experience.
  • Board includes industry veterans and experts in oncology and drug development.


About Recent Acquisition: Antev Ltd.


Antev Ltd. (“Antev”) is a clinical stage biotech company, developing Teverelix, a next generation GnRH antagonist, a potentially first in market product for high-risk prostate cancer patients and patients with first acute urinary retention (AUR) episodes due to enlarged prostate.


Antev’s flagship drug candidate is Teverelix trifluoroacetate (Teverelix TFA), a long-acting gonadotrophin-releasing hormone (GnRH) antagonist. Unlike GnRH agonists, which can cause an initial surge in testosterone levels, Teverelix directly suppresses sex hormone production without this surge, potentially reducing cardiovascular risks.


Teverelix: A Next-Gen GnRH Antagonist


Teverelix is being developed to compete with or improve upon current GnRH antagonists like Degarelix and Relugolix as well as agonists.


What sets Teverelix apart is the potential for:


  • Rapid onset of testosterone suppression and prostate shrinkage


  • Avoidance of testosterone flare versus agonists


  • A longer-acting injection schedule (possibly every 6 weeks)


  • Potential for subcutaneous and intra-muscular delivery without daily dosing (vs. Relugolix’s daily oral use)


  • Due to superior formulation, ISRs potentially significantly milder compared to Degarelix


What's Next for Teverelix?

Grab Key Sources: MDCX Presentation. MDCX Website.

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And as I mentioned previously, (Nasdaq: MDCX) has several potential catalysts that could generate breakout buzz. Check them out:


No. 1 MDCX Potential Catalyst - A Low Float Could Create The Environment For Heightened Volatility.


According to info from the Finviz websiteMDCX has a fairly low float.


The website reports this profile to have roughly 4.89Mn shares in its float.


Why is that important? It's important on one crucial level. Volatility potential.


If positive company news appears towards the end of 2025, could it provide a breakout spark when paired with the volatility potential of this low float?

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No. 2 MDCX Potential Catalyst - A Game-Changing Acquisition Gets Completed!


Medicus Pharma Ltd. Completes Acquisition of Antev Limited


Antev is developing Teverelix, a next generation GnRH Antagonist, as a first in class market product for Acute Urinary Retention (AURr) and high CV risk Prostate Cancer collecting representing ~US$6Bn in potential market opp.


Patrick J. Mahaffy, a veteran pharma executive and the former Chairman of Antev, appointed to Medicus Board of Directors


Philadelphia, Pennsylvania--(Newsfile Corp. - September 2, 2025) - Medicus Pharma Ltd. (NASDAQ: MDCX) ("Medicus" or the "Company"), ..., and Antev Limited ("Antev"), a UK-based clinical-stage drug development company, announced today that Medicus has acquired 98.6% of the issued and outstanding shares of Antev for aggregate consideration consisting of approximately US$2.97Mn in ca-sh and 1,603,164 common shares of Medicus, pursuant to the previously announced securities exchange agreement among Medicus, Antev and certain securityholders of Antev, dated as of June 29, 2025, as amended.


Antev is a clinical stage biotech company, developing Teverelix, a next generation GnRH antagonist, as a first in market product for cardiovascular high-risk prostate cancer patients and patients with first acute urinary retention (AURr) episodes due to enlarged prostate.


Antev's former shareholders will be entitled to receive up to approximately US$65Mn in additional contingent consideration tied to potential future FDA Phase 2 and New Drug Application approvals.


Following the completion of the acquisition, Patrick J. Mahaffy, a veteran pharma executive and the former chairman of Antev, was unanimously appointed to Medicus's board of directors. Mr. Mahaffy is also the former CEO of both Clovis Oncology (NASDAQ: CLVS) and Pharmion Corporation (NASDAQ: PHRM).


...


"We are delighted to complete the acquisition of Antev, which not only adds strategic depth to our drug development pipeline but also strengthens our team, both at the board and management level," stated Dr. Raza Bokhari, Medicus's Executive Chairman & CEO. "We believe, Teverelix, a next generation GnRH antagonist, is well positioned to become a first in class product to prevent acute urinary retention relapse due to enlarged prostate, and to treat advanced prostate cancer in patients with high cardiovascular risk profile, collectively representing approximately US$6Bn in potential market opp."


...


Read the full article here.

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No. 3 MDCX Potential Catalyst - An Average Of 6 Analyst Targets Suggest Major Upside Potential (Triple-Digit!).


Check out what MarketBeat is reporting:

As of Friday's close, MDCX had 6 analyst targets pointing to a significant amount of upside potential.


In fact, with an average target of $23.50, MDCX could have over 850% potential upside from its closing valuation last week.


MarketBeat reports further that Jason Kolbert of D. Boral Capital has given MDCX a $27 target representing a potential upside over 1,000% from Friday's close.


Additionally, the website shares Jason McCarthy of Maxim Group has provided a $20 target suggesting 700+% potential upside from Friday's close.


Could (Nasdaq: MDCX) be undervalued from current chart levels?

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No. 4 MDCX Potential Catalyst - Confidence Increases As Commercial Viability Could Come Into Focus In 2027.


Medicus Pharma Ltd. Receives Positive Feedback From the Food and Drug Adminstration (FDA) Type C Meeting Supporting the Development of Skinject


The FDA agrees that the Company may follow 505(b)(2) regulatory pathway to non-invasively treat basal cell carcinoma (BCC) of the skin using dissolvable Doxorubicin-containing Microneedle arrays (D-MNA) representing ~$2Bn in potential market opp.


The Company plans to complete patient recruitment for SKNJCT-003 before the end of Q4 2025 and to request End-of-Phase 2 (EOP2) with the FDA in Q1 2026


PHILADELPHIA, PENNSYLVANIA / ACCESS Newswire / September 29, 2025 / Medicus Pharma Ltd. (NASDAQ:MDCX) ("Medicus" or the "Company"), a biotech/life sciences company focused on advancing the clinical development programs of novel and potentially disruptive therapeutics assets, is pleased to announce positive feedback from Type C meeting with United States Food and Drug Administration (FDA).


The purpose of the Type C meeting was to discuss the design, endpoints, and other key protocol elements for the clinical development of doxorubicin containing microneedle array (D-MNA) to non-invasively treat basal cell carcinoma (BCC) of the skin.


The FDA provided clarity and further alignment that a relative bioavailability study with the Company's D-MNA product to treat BCC administered under certain conditions could provide support towards establishing a clinical bridge for the 505(b)(2) regulatory pathway as well as help satisfy the bioavailability requirement of the Company's D-MNA product as stated in 21CFR320.21. More specifically, the FDA provided positive and constructive feedback on a number of topics for the continued development of Skinject including, but not limited to: the appropriate primary endpoint for the next study; proposed patient population definition, including tumor size limits, location restrictions, and histological confirmation requirements; proposed randomized, double-blind, placebo-controlled, study design for future studies that are intended to demonstrate the effectiveness of D-MNA in treating BCC; and current safety assessments for the proposed study.


In anticipation of future pivotal studies, the FDA also provided recommendations to continue to optimize formulation and microneedle design, integrate an adhesive layer to affix the microneedle system to the body, and incorporate the use of an applicator to consistently apply the product to the application site.


"Establishing 505(b)(2) as a regulatory pathway to bring to market our novel, non-invasive Skinject D-MNA treatment to cure BCC of the skin, is a game changer," stated Dr. Raza Bokhari, Medicus's Executive Chairman & CEO, "by leveraging existing doxorubicin safety data, we will not only realize substantial drug development cost savings but also time savings compared to a traditional full development program. As we plan to complete patient recruitment for SKNJCT-003 before the end this year and request an EOP2 meeting with the FDA in Q1 2026, our confidence is increasing that Skinject may become commercially viable sometime in 2027."


...


Read the full article here.

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No. 5 MDCX Potential Catalyst - A Significant Update Shares Progression In Key Phase 2 Clinical Study.


Medicus Pharma Ltd. Provides Update on United Arab Emirates (UAE) SKNJCT-004 Phase 2 Clinical Study to Non-Invasively Treat Basal Cell Carcinoma of the Skin (BCC)


PHILADELPHIA, PENNSYLVANIA / ACCESS Newswire / September 8, 2025 / Medicus Pharma Ltd. (NASDAQ:MDCX) ("Medicus" or the "Company"), a biotech/life sciences company focused on advancing the clinical development programs of novel and potentially disruptive therapeutics assets, is pleased to announce that the SKNJCT-004 phase 2 clinical study, to non-invasively treat BCC of the skin, has commenced patient recruitment in Cleveland clinic Abu Dhabi (CCAD). Earlier this year, in May 2025, SKNJCT-004 received "study may proceed" approval from the UAE Department of Health.


The study is expected to randomize thirty-six (36) patients in four sites in UAE. In addition to Cleveland Clinic Abu Dhabi (CCAD), the study is also expected to commence patient recruitment in Sheikh Shakbout Medical City (SSMC), Burjeel Medical City (BMC), Rashid Hospital (RH), Clemenceau Medical Center (CMC) and American Hospital of Dubai (AHD).


Insights Research Organization and Solutions (IROS), a UAE-based contract research organization, is coordinating the clinical study for the Company. IROS is a M42 portfolio company.


"Commencing patient recruitment in the SKNJCT-004 clinical study at Cleveland Clinic Abu Dhabi is a promising step forward towards our goal to bring to market a first in class novel non-invasive alternative to treat BCC," stated Dr. Raza Bokhari, Medicus's Executive Chairman & CEO. "We have already randomized more than seventy five percent (75%) of the ninety (90) participants expected to be randomized in our AI powered SKNJCT-003 study, in the United States, which we believe represents more than US$2Bn in potential market opp."


...


Read the full article here.

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(Nasdaq: MDCX) Recap - These 5 Potential Breakout Catalysts Lead The Way


No. 1 - A Low Float Could Create The Environment For Heightened Volatility.


No. 2 - A Game-Changing Acquisition Gets Completed!


No. 3 - An Average Of 6 Analyst Targets Suggest Major Upside Potential (Triple-Digit!).


No. 4 - Confidence Increases As Commercial Viability Could Come Into Focus In 2027.


No. 5 - A Significant Update Shares Progression In Key Phase 2 Clinical Study.

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It's official. Coverage is now officially underway on Medicus Pharma Ltd. (Nasdaq: MDCX).


Updates will be on the way shortly. Keep your eyes peeled.


Sincerely,

Kai Parker

StockWireNews


(Always Remember The St-ock Prices Could Be Significantly Lower Now From The Dates I Provided.)


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