Allarity Therapeutics Inc (ALLR)

Hello to all, IMO I think the company is ready for bankruptcy, there has been no significant developments with stenoparvib. The predicted price target of 9 dollars at end of 2025 is bogus. Anyone dare to comment?

Like it again for another flip $1.63 think this round $2.80s as long as the dilution printing machines stay calm. Stop loss placed

Allarity Therapeutics (ALLR) Price Target Increased by 80.00% to $9.18

2025-08-06

The average one-year price target for Allarity Therapeutics (NasdaqCM:ALLR) has been revised to $9.18 / share. This is an increase of 80.00% from the prior estimate of $5.10 dated December 22, 2022.

The price target is an average of many targets provided by analysts. The latest targets range from a low of $9.09 to a high of $9.45 / share. The average price target represents an increase of 783.54% from the latest reported closing price of $1.04 / share.

What is the Fund Sentiment?
There are 12 funds or institutions reporting positions in Allarity Therapeutics. This is an increase of 3 owner(s) or 33.33% in the last quarter. Average portfolio weight of all funds dedicated to ALLR is 0.00%, an increase of 93.86%. Total shares owned by institutions increased in the last three months by 9.77% to 126K shares.

What are Other Shareholders Doing?
Geode Capital Management holds 34K shares representing 0.22% ownership of the company.

FSMAX - Fidelity Extended Market Index Fund holds 27K shares representing 0.18% ownership of the company. In its prior filing, the firm reported owning 7K shares , representing an increase of 73.70%. The firm increased its portfolio allocation in ALLR by 332.40% over the last quarter.

Corsair Capital Management holds 20K shares representing 0.13% ownership of the company.

Barclays holds 10K shares representing 0.07% ownership of the company.

FCFMX - Fidelity Series Total Market Index Fund holds 7K shares representing 0.04% ownership of the company. In its prior filing, the firm reported owning 3K shares , representing an increase of 50.94%. The firm increased its portfolio allocation in ALLR by 105.60% over the last quarter.

https://fintel.io/news/allarity-therapeutics-allr-price-target-increased-by-8000-to-918-496

(Targets are not always met)

$ALLR

Congestion $2.10- $2.30s but if it breaks that zone straight to $2.88- $3

2.06 !!

$ALLR - News Out - Allarity Therapeutics Granted FDA Fast Track Designation for Stenoparib for the Treatment of Advanced Ovarian Cancer
https://www.globenewswire.com/news-release/2025/08/26/3139198/0/en/Allarity-Therapeutics-Granted-FDA-Fast-Track-Designation-for-Stenoparib-for-the-Treatment-of-Advanced-Ovarian-Cancer.html

All out $1.63 take those gains any day

Like it in some looking at $1.70 for flip or just a little sooner but $2.20s another possible zome

Pump it 1.09

$ALLR - Stockta Technical analysis review : https://stockta.com/cgi-bin/analysis.pl?symb=ALLR&mode=stock

$ALLR News : Allarity Therapeutics Receives Australian Patent Acceptance Notice for Stenoparib DRP® Companion Diagnostic
TARPON SPRINGS, Fla., June 30, 2025 -- Allarity Therapeutics, Inc. (“Allarity” or the “Company”) (NASDAQ: ALLR), a Phase 2 clinical-stage pharmaceutical company dedicated to developing stenoparib—a differentiated, dual PARP and WNT pathway inhibitor—as a personalized cancer treatment using its proprietary, drug-specific Drug Response Predictor (DRP®) patient selection technology—today announced that IP Australia, the Australian Government agency that administers intellectual property rights in the country, has formally accepted the Company’s patent application for its DRP® companion diagnostic specific to stenoparib.

https://finance.yahoo.com/news/allarity-therapeutics-receives-australian-patent-120000173.html

Allarity Therapeutics (ALLR): A Biotech Turnaround With FDA Fast-Track Potential

$ALLR - @Barchart























https://www.barchart.com/stocks/quotes/ALLR/cheat-sheet

$ALLR Breaking News : Allarity Therapeutics Announces Research Collaboration with Indiana Biosciences Research Institute to Further Advance Understanding of Stenoparib’s Unique, Dual Therapeutic Mechanism of Action
TARPON SPRINGS, Fla., June 4, 2025 -- Allarity Therapeutics, Inc. (“Allarity” or the “Company”) (NASDAQ: ALLR), a Phase 2 clinical-stage pharmaceutical company dedicated to developing stenoparib—a differentiated, dual PARP and WNT pathway inhibitor—as a personalized cancer treatment using its proprietary, drug-specific Drug Response Predictor (DRP®) patient selection technology—today announced a research collaboration with the Indiana Biosciences Research Institute (IBRI). The collaboration is aimed primarily at further deepening the Company’s mechanistic understanding of the dual mechanism of action of stenoparib.

https://finance.yahoo.com/news/allarity-therapeutics-announces-research-collaboration-120000202.html

$ALLR Barchart
https://www.barchart.com/stocks/quotes/ALLR/cheat-sheet

News Update $ALLR Allarity Therapeutics Announces First Patient Enrolled in New Phase 2 Clinical Trial Protocol of Stenoparib in Advanced Ovarian Cancer

TARPON SPRINGS, Fla., June 2, 2025 -- Allarity Therapeutics, Inc. (“Allarity” or the “Company”) (NASDAQ: ALLR), a Phase 2 clinical-stage pharmaceutical company dedicated to developing stenoparib—a differentiated, dual PARP and WNT pathway inhibitor—today announced that the first patient has been enrolled in its new Phase 2 clinical trial protocol of stenoparib for the treatment of advanced, platinum-resistant or platinum-ineligible ovarian cancer.

The newly launched protocol will accelerate the clinical development of stenoparib and its drug-specific Drug Response Predictor (DRP®) companion diagnostic (CDx) toward potential FDA approval. It builds on encouraging data from Allarity’s earlier and still ongoing Phase 2 study, which demonstrated that patients on twice-daily stenoparib showed durable clinical benefit and that stenoparib was well tolerated. Two patients remain on treatment and continue to derive benefit after more than 20 months. Reflecting the compelling and durable clinical responses observed in platinum-resistant patients to date, the new trial protocol specifically focuses on evaluating stenoparib in patients with advanced, recurrent, platinum-resistant, or platinum-ineligible ovarian cancer—patients for whom current treatment options are extremely limited and typically involve additional chemotherapy, which is associated with well-documented side effects.

“With the enrollment of the first patient, we are fulfilling our promise to accelerate stenoparib’s clinical development as a potentially safer, more effective alternative to chemotherapy for women with advanced, recurrent ovarian cancer,” said Thomas Jensen, Chief Executive Officer of Allarity Therapeutics. “This new protocol reflects critical input from leading gynecologic oncologists, and allows us to solidify the importance of DRP for patients who are most likely to receive clinical benefit from stenoparib. This study also allows us to confirm and extend our current findings that show clinical benefit from twice daily dosing.”

In addition to assessing overall efficacy and safety, the new trial protocol is designed to further advance the Company’s understanding of stenoparib’s modulation of the WNT signaling pathway—a key driver of disease progression in ovarian and other cancers. The Company is actively pursuing ways to deepen its insights into the therapeutic importance of this WNT-modulating activity and how this, in addition to a cleaner safety profile, distinguishes stenoparib from first-generation PARP inhibitors.

Building on the clinical benefit of the current dosing schedule, this updated study design also includes an additional dosing level to explore the optimal dose for enhancing clinical benefit, aligning Allarity with the FDA’s Project Optimus initiative to inform the start of pivotal registration trials.

The trial is expected to generate significant clinical data by late summer 2026. Allarity plans to pursue multiple advantaged regulatory pathways to expedite potential approval of both stenoparib and its DRP companion diagnostic (CDx).

About Stenoparib
Stenoparib is an orally available, small-molecule dual-targeted inhibitor of PARP1/2 and tankyrase 1/2. At present, tankyrases are attracting significant attention as emerging therapeutic targets for cancer, principally due to their role in regulating the Wnt signaling pathway. Aberrant Wnt/ß-catenin signaling has been implicated in the development and progression of numerous cancers. By inhibiting PARP and blocking Wnt pathway activation, stenoparib’s unique therapeutic action shows potential as a promising therapeutic for many cancer types, including ovarian cancer. Allarity has secured exclusive global rights for the development and commercialization of stenoparib, which was originally developed by Eisai Co. Ltd. and was formerly known under the names E7449 and 2X-121.

About the Drug Response Predictor – DRP® Companion Diagnostic
Allarity uses its drug-specific DRP® to select those patients who, by the gene expression signature of their cancer, may have a high likelihood of benefiting from a specific drug. By screening patients before treatment, and only treating those patients with a sufficiently high, drug-specific DRP score, the therapeutic benefit rate may be enhanced. The DRP method builds on the comparison of sensitive vs. resistant human cancer cell lines, including transcriptomic information from cell lines, combined with clinical tumor biology filters and prior clinical trial outcomes. DRP is based on messenger RNA expression profiles from patient biopsies. The DRP® platform has shown an ability to provide a statistically significant prediction of the clinical outcome from drug treatment in cancer patients across dozens of clinical studies (both retrospective and prospective). The DRP platform, which may be useful in all cancer types and is patented for dozens of anti-cancer drugs, has been extensively published in the peer-reviewed literature.

About Allarity Therapeutics
Allarity Therapeutics, Inc. (NASDAQ: ALLR) is a clinical-stage biopharmaceutical company dedicated to developing personalized cancer treatments. The Company is focused on development of stenoparib, a novel PARP/tankyrase inhibitor for advanced ovarian cancer patients, using its DRP® technology to develop a companion diagnostic that can be used to select those patients expected to derive the greatest clinical benefit from stenoparib. Allarity is headquartered in the U.S., with a research facility in Denmark, and is committed to addressing significant unmet medical needs in cancer treatment. For more information, visit www.allarity.com.

Follow Allarity on Social Media
LinkedIn: https://www.linkedin.com/company/allaritytx/

Forward-Looking Statements
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements provide the Company’s current expectations or forecasts of future events. The words “anticipates,” “believe,” “continue,” “could,” “estimate,” “expect,” “intends,” “may,” “might,” “plan,” “possible,” “potential,” “predicts,” “project,” “should,” “would” and similar expressions may identify forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking. These forward-looking statements include, but are not limited to, statements related to the initiation, conduct, and expected outcomes of the new Phase 2 clinical trial protocol for stenoparib in advanced, platinum-resistant or platinum-ineligible ovarian cancer; the potential for stenoparib to demonstrate improved safety, tolerability, or efficacy compared to existing treatments; the evaluation of WNT pathway modulation as a mechanism of action; the development and potential regulatory approval of the Company’s DRP® companion diagnostic; the alignment of the trial design with FDA initiatives such as Project Optimus; and anticipated timing of future clinical data readouts and regulatory submissions. Any forward-looking statements in this press release are based on management’s current expectations of future events and are subject to multiple risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to, the risk that stenoparib may not demonstrate sufficient clinical benefit or safety in the updated Phase 2 trial protocol; the risk that patient enrollment, site activation, or data collection may be delayed or disrupted; the risk that earlier clinical observations may not be confirmed in larger patient populations; the possibility that the DRP® companion diagnostic may not be validated, approved, or adopted; and the risk that regulatory pathways or agency feedback may not support accelerated approval or market access. For a discussion of other risks and uncertainties, and other important factors, any of which could cause our actual results to differ from those contained in the forward-looking statements, see the section entitled “Risk Factors” in our Form 10-K annual report filed with the Securities and Exchange Commission (the “SEC”) on March 31, 2025, available at the SEC’s website at www.sec.gov, and as well as discussions of potential risks, uncertainties and other important factors in the Company’s subsequent filings with the SEC. All information in this press release is as of the date of the release, and the Company undertakes no duty to update this information unless required by law.

###

Company Contact:
investorrelations@allarity.com


Media Contact:
Thomas Pedersen
Carrotize PR & Communications
+45 6062 9390
tsp@carrotize.com

Attachment

Allarity Therapeutics Press Release - First Patient Enrolled in New Phase 2 Clinical Trial Protocol

https://finance.yahoo.com/news/allarity-therapeutics-announces-first-patient-120000390.html

$ALLR - About the company: Overview
https://allarity.com/about-us/

$ALLR Allarity Therapeutics Corporate Presentation 2025 Q1 https://allarity.com/wp-content/uploads/2025/03/ALLR_March_2025.pdf

https://allarity.com/about-us/

ALLR

https://www.globenewswire.com/news-release/2025/05/09/3078515/0/en/Allarity-Therapeutics-Provides-First-Quarter-2025-Update-Highlighting-Continued-Stenoparib-Benefit-and-Upcoming-Trial-Enrollment.html

$ALLR Allarity Therapeutics Presents Novel Drug Response Predictor—DRP®—for Daratumumab in Multiple Myeloma at AACR 2025
TARPON SPRINGS, Fla., April 25, 2025 -- Allarity Therapeutics, Inc. (“Allarity” or the “Company”) (NASDAQ: ALLR), a Phase 2 clinical-stage pharmaceutical company dedicated to developing stenoparib—a differentiated, dual PARP and WNT pathway inhibitor—as a personalized cancer treatment using its proprietary, drug-specific Drug Response Predictor (DRP®) patient selection technology today announced the presentation of a poster containing data on a new DRP for the monoclonal antibody drug daratumumab. The poster is to be presented during a session at the 2025 American Association for Cancer Research (AACR) Annual Meeting, taking place April 25–30, 2025, in Chicago, IL. This novel predictor is designed to identify multiple myeloma patients most likely to benefit from daratumumab.

https://finance.yahoo.com/news/allarity-therapeutics-presents-novel-drug-120000942.html

Williams was Oversold...🥳...looks like a reset...

Started off strong yesterday, but sliding today. Maybe yesterday was folks buying in ahead of news?
Anyway, chart still good and RSI is cooling down a bit.

ALLR: Added @ 1.03

$ALLR Allarity Therapeutics is a clinical-stage precision medicine company actively advancing stenoparib, an orally available, small molecule inhibitor for patients with advanced recurrent ovarian cancer. The company is leveraging its proprietary, highly accurate Drug Response Predictor (DRP®) technology to refine patient selection and improve clinical outcomes. Publicly traded on NASDAQ, Allarity (ALLR) is headquartered in Boston, MA, while maintaining an R&D facility in Hoersholm, Denmark. Allarity is committed to enhancing patient outcomes through improved decision-making and personalized cancer care.

https://allarity.com/

Thank you...Enjoy the 3 day weekend...🥳

Bidding more in the AH's. See what happens
Have a Good One georgie

Patience...🥳

Finally

ALLR...93...HOD...🥳...Psar flipped Bullish...

Dismal performance.

I got out even at 1.10. Good thing is, it is not a shit company, it just pumped up by high expectations, that the call would reveal something good.
Turns out, it's just going to take longer than anticipated. In other words, not ahead of normal.

Guess I should of taken the $1.20 when it was there!

ALLR: Call not so impressive I guess. 🙄

Will be looking for news tomorrow or monday covering today's conference... $ALLR

Holding strong here

So far, looks like today was a warmup lap. May take off in the AH's?

CMF turning up

$ALLR Chart turning more bullish. RSI getting stronger here. MACD bullish cross. Get through $1.20 and we can see $2 pretty quick here. 🚀

Event on March 27th: Predicting The Success Of Potential Cancer Treatments ~ $ALLR https://forcefamilyoffice.com/events/healthcare/allarity-therapeutics-coming-march-27-2025/

Is there likely nss being done here?

$ALLR Big News Out!! Allarity Therapeutics Launches Comprehensive Effort to Combat Potential Illegal Naked Short Selling of Its Shares https://finance.yahoo.com/news/allarity-therapeutics-launches-comprehensive-effort-120000774.html

ALLR...$1.01...🥳...Reversing here...

Onward and upward!

$ALLR Trial to explore novel combination therapy for patients with recurrent Small Cell Lung Cancer who have failed frontline treatment
Fully funded by the U.S. Veterans’ Administration Special Emphasis Panel on Precision Oncology
Trial builds on promising clinical evidence supporting a PARP inhibitor and temozolomide combination in Small Cell Lung Cancer
https://finance.yahoo.com/news/allarity-therapeutics-announces-phase-2-130000563.html

How much is a fully funded P2 Trial $20M-$30M ??

When we hit 5M volume look out above

Nice volume getting serious

https://substack.com/inbox/post/158047254?utm_campaign=post&triedRedirect=true

50 - 100% potential here next week