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Propanc Biopharma Provides Corporate Update and Reports Third Quarter 2025/26 Results

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Propanc Biopharma (Nasdaq:PPCB) reported Q3 2025/26 results and key corporate milestones. The company is advancing lead asset PRP toward a Phase 1b first-in-human study in advanced solid tumor patients and strengthening its anti-aging and cancer research portfolio via a multi-year Spanish university collaboration.

Propanc entered a private placement for up to $100 million, received $2 million by March 31 plus a subsequent $0.5 million tranche, reduced liabilities by $2.10 million and cut convertible notes to $55,000, ending the quarter with $14.33 million in assets and $443,702 in cash.

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AI-generated analysis. Not financial advice.

Positive

  • Private placement facility for up to $100 million to accelerate clinical development
  • Total liabilities reduced by $2.10 million in the quarter
  • Convertible notes cut to $55,000 from $538,000
  • Net cash from financing activities of $4.47 million
  • Quarter-end total assets of $14.33 million
  • Service and research agreements support PRP clinical readiness and new anti-aging IP

Negative

  • Quarter-end cash balance limited to $443,702 despite new financing
  • Ongoing operations and R&D depend on continued access to the financing facility

News Market Reaction – PPCB

-6.98%
6 alerts
-6.98% News Effect
-19.0% Trough in 9 hr 39 min
-$120K Valuation Impact
$1.60M Market Cap
1.1x Rel. Volume

On the day this news was published, PPCB declined 6.98%, reflecting a notable negative market reaction. Argus tracked a trough of -19.0% from its starting point during tracking. Our momentum scanner triggered 6 alerts that day, indicating moderate trading interest and price volatility. This price movement removed approximately $120K from the company's valuation, bringing the market cap to $1.60M at that time.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Private placement facility: $100 million Initial Series C investment: $1,000,000 Follow-on Series C investment: $1,000,000 +5 more
8 metrics
Private placement facility $100 million Maximum size of private placement agreement to accelerate clinical development
Initial Series C investment $1,000,000 Received upon issuance of 100 shares of Series C Convertible Preferred Stock
Follow-on Series C investment $1,000,000 Received by March 31, 2026 upon exercise of 100 Series C Preferred shares
Total assets $14.33 million Quarter ended March 31, 2026
Liabilities reduction $2.10 million Total liabilities reduced by this amount in Q3 2025/26
Convertible notes balance $55,000 (from $538,000) Convertible notes reduced as of March 31, 2026
Net cash from financing $4.47 million Net cash provided by financing activities in the quarter
Quarter-end cash $443,702 Cash balance at March 31, 2026; excludes later $0.5M tranche

Market Reality Check

Price: $1.3700 Vol: Volume 3,356,332 is 2.35x...
high vol
$1.3700 Last Close
Volume Volume 3,356,332 is 2.35x the 20-day average of 1,429,558, indicating elevated trading interest ahead of and around this update. high
Technical Price 0.0731 is far below the 200-day MA 1.36 and sits 99.34% below the 52-week high of 11, only modestly above the 52-week low of 0.0651.

Peers on Argus

PPCB fell 21.4% while close peers showed mixed, mostly modest moves (e.g., AKTX ...
1 Up 1 Down

PPCB fell 21.4% while close peers showed mixed, mostly modest moves (e.g., AKTX +8.82%, LIXT +1.61%, ALLR -3.23%, RNTX -2.59%, BOLD 0%). Momentum scanner data also flags mixed peer directions, pointing to a stock-specific reaction rather than a coordinated biotech sector move.

Historical Context

5 past events · Latest: May 13 (Neutral)
Pattern 5 events
Date Event Sentiment Move Catalyst
May 13 Reverse stock split Neutral -21.4% 1-for-25 reverse split to help regain Nasdaq $1 bid compliance.
Mar 24 Research collaboration Positive -5.9% Multi-year anti-aging and cancer research deal with Spanish universities.
Mar 12 Preclinical efficacy data Positive -13.6% Preclinical PRP data showing >85% tumor inhibition and plan for FIH trials.
Mar 10 PK assay agreement Positive -20.5% Service agreement with FyoniBio to develop an LC-MS PK assay for PRP.
Mar 03 Program overview Positive -5.2% Update on PRP preclinical profile, orphan status, funding facility and FIH plans.
Pattern Detected

Recent history shows PPCB often trading lower after ostensibly positive corporate, financing, and R&D announcements, suggesting a pattern of negative price reactions to news.

Recent Company History

Over the last six months, Propanc Biopharma issued several updates around PRP and financing. In March 2026, it highlighted >85% tumor growth inhibition data and plans for a Phase 1b FIH trial, plus an LC‑MS PK assay agreement and a multi‑year Spanish research collaboration, yet shares fell after each release. A May 18, 2026 reverse stock split to support Nasdaq compliance also saw a sharp decline. Today’s quarterly and corporate update, including use of a large financing facility, arrives against this backdrop of repeated selloffs following news.

Market Pulse Summary

The stock moved -7.0% in the session following this news. The decline reflects ongoing skepticism de...
Analysis

The stock moved -7.0% in the session following this news. The decline reflects ongoing skepticism despite updates on PRP’s advancement and added financing, including a facility up to $100 million and Q3 cash of $443,702. Historically, PPCB has often traded lower after positive-sounding news, with several March 2026 announcements followed by declines of 5–20%. Persistent losses, equity-linked financing, and a very low share price relative to the 200-day MA 1.36 could leave the stock vulnerable to continued pressure.

Key Terms

pharmacokinetics, liquid chromatography-mass spectrometry (LC-MS), first-in-human (FIH), senescence, +4 more
8 terms
pharmacokinetics medical
"validating a liquid chromatography-mass spectrometry (LC-MS) based pharmacokinetics (PK) assay"
Pharmacokinetics is the study of how a substance, such as a drug or chemical, moves through and is processed by the body over time. It tracks how it is absorbed, distributed, broken down, and eventually eliminated. For investors, understanding pharmacokinetics helps gauge the effectiveness, safety, and potential risks of new medications or treatments, which can influence a company’s success and valuation in the healthcare industry.
liquid chromatography-mass spectrometry (LC-MS) technical
"establishing and validating a liquid chromatography-mass spectrometry (LC-MS) based PK assay"
An analytical lab technique that first separates a mixture into its components (like passing a soup through finer and finer sieves) and then measures each component’s unique mass signature (like taking a molecular fingerprint). Investors care because LC-MS is a primary tool for verifying drug purity, detecting trace contaminants, measuring biomarker levels in trials, and supporting regulatory filings—results that affect a product’s safety, approval prospects, and commercial value.
first-in-human (FIH) medical
"Phase 1b, First-In-Human (FIH) study in advanced cancer patients"
The first-in-human (FIH) designation marks the first time a new drug, vaccine, medical device, or treatment is given to people rather than tested only in labs or animals. For investors, FIH is a major milestone because it moves a candidate from preclinical testing into human safety and early effectiveness evaluation—think of it as the prototype being driven on public roads, where results strongly influence future development costs, timelines, and commercial potential.
senescence medical
"evaluation of a senescence-modulating (i.e., anti-aging) compound to mitigate senescence"
Senescence is the process by which cells stop dividing and enter a long-term, inactive state while remaining alive and sending signals to their neighbors. Think of senescent cells as retired workers who no longer perform useful tasks but clutter the workplace and call attention to problems; they can drive inflammation, tissue decline, and disease. For investors, senescence matters because it is a key target for drugs and diagnostics in aging-related and chronic diseases, influencing the potential size, risk, and timeline of biotech investments.
proenzymes medical
"lead asset, PRP, consisting of two proenzymes trypsinogen and chymotrypsinogen"
Proenzymes are inactive precursors of enzymes that become functional only after a specific chemical change, often involving cutting part of the molecule, similar to removing a safety cover on a tool to make it usable. They matter to investors because drugs, diagnostics, and manufacturing processes that rely on proenzymes can have different effectiveness, safety profiles, storage needs, and production costs than products that use already-active enzymes, which can affect clinical outcomes, regulatory decisions, and commercial value.
GMP technical
"engaging with CDMOs for the GMP manufacture of PRP for supply"
Good Manufacturing Practice (GMP) is a set of regulatory standards and procedures that ensure products—especially medicines, medical devices, and related goods—are consistently made to meet safety, quality, and purity requirements. For investors, GMP compliance is like a factory’s hygiene and checklist system: it reduces the risk of product recalls, regulatory fines, and production stoppages, supports market access, and signals more reliable, lower-risk operations that can protect revenue and reputation.
CROs technical
"CROs (Clinical Research Organizations) to discuss management of future clinical trial operations"
Contract research organizations (CROs) are independent firms hired by drug and medical-device companies to run research tasks such as clinical trials, patient recruitment, lab testing, data management, and regulatory filings. For investors they matter because CROs act like contractors turning a sponsor’s plans into finished work—so their capacity, timelines, costs and quality directly affect how quickly and cheaply a drug or device can move toward approval and revenue.
CDMOs technical
"management is engaging with CDMOs (Contract Development and Manufacturing Organizations)"
Contract Development and Manufacturing Organizations (CDMOs) are independent companies that help drug and biologic developers by designing, testing, scaling up and producing medicines on a contract basis — think of them as a hired factory and research partner that turns a medical idea into a manufacturable product. They matter to investors because they provide steady, service-based revenue, spread development and production risk for drug makers, and their capacity, quality and pricing can directly affect the speed and cost of getting medicines to market.

AI-generated analysis. Not financial advice.

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Entering a Transformative Stage by Advancing PRP to a Pivotal, Phase 1b, FIH, Clinical Study Whilst Undertaking Additional Research into Age-Related Chronic Diseases

MELBOURNE, Australia, May 15, 2026 (GLOBE NEWSWIRE) -- Propanc Biopharma, Inc. (Nasdaq: PPCB) (“Propanc” or the “Company”), a biopharmaceutical company focused on developing novel treatments for chronic diseases, including recurrent and metastatic cancer, today announced an update on corporate progress and reported third quarter financial results as of March 31, 2026 (Year end June 30).

Corporate and R&D Highlights

Executes Service Agreement with FyoniBio GmbH to Establish & Validate Pharmacokinetics Assay for Phase 1b First-In-Human Study

Management has executed a service agreement with FyoniBio GmbH (formerly Glycotope, est. 2010), a German Contract Development Organization (CDO) based in Berlin for establishing and validating a liquid chromatography-mass spectrometry (LC-MS) based pharmacokinetics (PK) assay. The objective is to quantify the Company’s lead asset, PRP, consisting of two proenzymes trypsinogen and chymotrypsinogen, as well as their activated enzyme forms trypsin and chymotrypsin from human serum during the Phase 1b, First-In-Human (FIH) study in advanced cancer patients suffering from solid tumors.

Executes Multi-Yr, Anti-Aging & Cancer Research Collaboration with the Universities of Jaén and Granada, Spain

A multi-year Joint Research Collaboration Agreement has been established with the Universities of Jaén (UJA) and Granada (UGR), Spain. The collaboration involves the evaluation of a senescence-modulating (i.e., anti-aging) compound to mitigate senescence and to complete experiments to further support the claims of recently filed fibrosis and cancer related patent applications, requested by Propanc Biopharma Inc. to the research group “Biological Technologies of The University of Jaén” and UGR’s Research Group, “Advanced Therapies: Differentiation, Regeneration and Cancer.”

Corporate and Financial Updates

Propanc entered into a private placement agreement for up to $100 million to accelerate clinical development. The Company received an initial $1,000,000 investment upon issuance of 100 shares of Series C Convertible Preferred Stock. As of March 31st, a further $1,000,000 investment was received upon exercise of 100 shares of Series C Convertible Preferred Stock.

Q3 Financial Summary (Quarter Ended March 31, 2026)

  • Total assets: $14.33 million

  • Total liabilities reduced by $2.10 million

  • Convertible notes reduced to $55,000 (from $538,000)

  • Net cash from financing activities: $4.47 million

  • Quarter-end cash: $443,702

  • $0.5 million tranche from the Series C facility subsequently received

The Company expects the financing facility to continually support planned R&D activities, including advancement of PRP and Rec-PRP.

Management Commentary

“We are entering a pivotal phase of development for the Company’s lead asset, PRP, which is progressing to a world first, Phase 1b, First-In-Human study, in 30 – 40 advanced cancer patients suffering from solid tumors. Execution of an agreement with Fyoni Bio will facilitate method development and validation of the pharmacokinetics method in preparation for the pivotal clinical study. In addition, management is engaging with CDMOs (Contract Development and Manufacturing Organizations) for the GMP manufacture of PRP for supply of the finished drug product, CROs (Clinical Research Organizations) to discuss management of future clinical trial operations, as well as preparing regulatory documentation for the Clinical Trial Application targeting submission later this year,” said Mr. James Nathanielsz, Propanc’s Chief Executive Officer. “Additionally, our multi-year research agreement with the Universities of Jaén and Granada will continue to support, strengthen and grow our intellectual property around the use of proenzymes not just in cancer, but also focusing on cell rejuvenation to overcome age-related, chronic diseases, such as fibrosis. I am confident we are on the right path to execute a rapid transformation of our Company to clinical stage for a range of incurable diseases which can offer renewed hope for patients.”

About Propanc Biopharma, Inc.

Propanc Biopharma, Inc. (Nasdaq: PPCB) is developing a novel approach to preventing cancer recurrence and metastasis by targeting and eradicating cancer stem cells through proenzyme activation. The Company’s lead product candidate, PRP, is designed to address the underlying drivers of cancer proliferation and spread.

More information: www.propanc.com

Forward-Looking Statements

All statements in this press release that are not historical are forward-looking statements, including, among other things, statements relating to the Company’s expectations regarding its market position and market opportunity, expectations and plans as to its product development, manufacturing and sales, and relations with its partners and investors, made in reliance upon the safe harbor provisions of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These statements are not historical facts but rather are based on the Company’s current expectations, estimates, and projections regarding its business, operations and other similar or related factors. Words such as “may,” “will,” “could,” “would,” “should,” “anticipate,” “predict,” “potential,” “continue,” “expect,” “intend,” “plan,” “project,” “believe,” “estimate,” and other similar or related expressions are used to identify these forward-looking statements, although not all forward-looking statements contain these words. You should not place undue reliance on forward-looking statements because they involve known and unknown risks, uncertainties, and assumptions that are difficult or impossible to predict and, in some cases, beyond the Company’s control. Forward-looking statements are not guarantees of future actions or performance. Actual results may differ materially from those in the forward-looking statements because of several factors, including, without limitation, risks and uncertainties related to market conditions, as well as those risks described under “Risk Factors” in the prospectus related to the proposed offering and those described in the Company’s filings with the SEC. The Company undertakes no obligation to revise or update information in this release to reflect events or circumstances in the future, even if new information becomes available.

Company:
Propanc Biopharma, Inc.
James Nathanielsz
+61-3-9882-0780
info@propanc.com

Investor Contact:
irteam@propanc.com

PROPANC BIOPHARMA, INC. AND SUBSIDIARY
CONDENSED CONSOLIDATED BALANCE SHEETS
 
 March 31, 2026
 June 30, 2025
 (Unaudited)
  
ASSETS 
 
CURRENT ASSETS:
Cash$443,702  $12,088 
GST tax receivable 11,057   5,302 
Prepaid expenses - current portion 7,733,625   8,334,046 
Other current assets 35,104   1,380 
        
TOTAL CURRENT ASSETS 8,223,488   8,352,816 
        
Deferred offering costs -   291,773 
Prepaid expenses - long-term portion 6,057,422   10,925,835 
Security deposit - related party 2,065   1,971 
Operating lease right-of-use assets, net - related party 46,584   59,413 
Property and equipment, net 4,221   - 
 
TOTAL ASSETS$14,333,780  $19,631,808 
 
LIABILITIES AND STOCKHOLDERS’ EQUITY 
 
CURRENT LIABILITIES:
Accounts payable$973,692  $1,249,596 
Accrued expenses and other payables 942,376   1,486,550 
Accrued interest 123,181   190,795 
Loans payable -   65,280 
Loans payable - related parties, net of discount 465,282   415,329 
 
Notes payable, net of discount -   543,312 
Convertible notes, net of discounts and including put premiums 55,000   537,921 
Operating lease liability - related party, current portion 23,324   17,664 
Warrant liability 104,313   - 
Embedded conversion option liabilities 50,273   403,892 
Employee benefit liability 738,187   667,901 
 
TOTAL CURRENT LIABILITIES 3,475,628   5,578,240 
 
NON-CURRENT LIABILITIES:
Loan payable - long-term - related party, net of discount -   105,627 
Operating lease liability - long-term portion - related party 30,267   41,749 
 
TOTAL NON-CURRENT LIABILITIES 30,267   147,376 
 
TOTAL LIABILITIES$3,505,895  $5,725,616 
 
Temporary Equity – Convertible Preferred Stock Series C - $0.01 par value, $10,000 stated value, 9,900 shares designated and authorized, 100 (liquidation value of $1,000,000) and none issued and outstanding at March 31, 2026 and June 30, 2025, respectively$1,000,000  $- 
 
Commitments and Contingencies (See Note 9)
 
STOCKHOLDERS’ EQUITY:
Preferred stock, 1,500,005 shares authorized, $0.01 par value:
Series A preferred stock, $0.01 par value; 500,000 shares previously authorized; 0 shares issued and outstanding as of March 31, 2026 and June 30, 2025$-  $- 
Series B preferred stock, $0.01 par value; 5 shares authorized; 1 share issued and outstanding as of March 31, 2026 and June 30, 2025 -   - 
 
Common stock, $0.001 par value; 10,000,000,000 shares authorized; 21,859,281 and 11,611,782 shares issued and outstanding as of March 31, 2026 and June 30, 2025, respectively 21,860   11,612 
Common stock issuable (33,007,750 and 7,750 shares as of March 31, 2026 and June 30, 2025, respectively) 33,008   8 
Additional paid-in capital 149,427,962   138,243,652 
Accumulated other comprehensive income 1,234,766   1,318,917 
Accumulated deficit (140,843,234)  (125,621,520)
Treasury stock ($0.001 share) (46,477)  (46,477)
 
TOTAL STOCKHOLDERS’ EQUITY 9,827,885   13,906,192 
 
TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY$14,333,780  $19,631,808 
 


PROPANC BIOPHARMA, INC. AND SUBSIDIARY
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE INCOME (LOSS)
(Unaudited)
 
 For the three months
ended March 31,

 For the nine months
ended March 31,

 2026
 2025
 2026
 2025
 
REVENUE
Revenue$-  $-  $-  $- 
 
OPERATING EXPENSES
Administration expenses (including noncash compensation expense of $11,581,251 and $52,853,115 for the nine months ended March 31, 2026 and 2025, respectively, and $5,351,136 and $52,838,115 for the three months ended March 31, 2026 and 2025, respectively. 6,219,644   53,068,147   14,446,391   53,442,499 
Occupancy expenses - related party 10,917   6,469   32,306   20,187 
Research and development 169,660   54,097   249,822   170,199 
TOTAL OPERATING EXPENSES 6,400,221   53,128,713   14,728,519   53,632,885 
 
LOSS FROM OPERATIONS (6,400,221)  (53,128,713)  (14,728,519)  (53,632,885)
 
OTHER INCOME (EXPENSE)
Interest expense (38,270)  (104,042)  (402,874)  (309,215)
Interest income 13   1   69   2 
Derivative expense -   (59,271)  -   (95,012)
Change in fair value of derivative liabilities (18,146)  47,119   49,876   113,487 
Change in fair value of warrant liability 182,517   -   776,227   - 
Other expense 43,000   -   (11,000)  - 
Settlement expense (90,000)  -   (90,000)  - 
Gain (loss) on extinguishment of debt, net (74,235)  (809,954)  135,943   (840,032)
Foreign currency transaction gain (loss) 35,006   (12,486)  (19,190)  (88,184)
TOTAL OTHER INCOME (EXPENSE), NET 39,885   (938,633)  439,051   (1,218,954)
 
LOSS BEFORE TAXES (6,360,336)  (54,067,346)  (14,289,468)  (54,851,839)
 
Tax benefit -   -   -   - 
 
NET LOSS$(6,360,336) $(54,067,346) $(14,289,468) $(54,851,839)
 
Deemed Dividend -   -   (932,246)  - 
 
NET LOSS AVAILABLE TO COMMON STOCKHOLDERS$(6,360,336) $(54,067,346) $(15,221,714) $(54,851,839)
 
BASIC AND DILUTED NET LOSS PER SHARE$(0.28) $(12.50) $(0.95) $(38.62)
 
BASIC AND DILUTED WEIGHTED AVERAGE SHARES OUTSTANDING 22,427,486   4,325,994   15,973,535   1,420,307 
 
NET LOSS$(6,360,336) $(54,067,346) $(15,221,714) $(54,851,839)
 
OTHER COMPREHENSIVE INCOME (LOSS)
Unrealized foreign currency translation gain (loss) (93,349)  (27,311)  (84,151)  194,976 
 
TOTAL OTHER COMPREHENSIVE INCOME (LOSS) (93,349)  (27,311)  (84,151)  194,976 
 
TOTAL COMPREHENSIVE LOSS$(6,453,685) $(54,094,657) $(15,305,865) $(54,656,863)



FAQ

What corporate updates did Propanc Biopharma (Nasdaq:PPCB) announce on May 15, 2026?

Propanc Biopharma announced Q3 2025/26 results, new financing, and R&D milestones. According to Propanc, it is advancing PRP toward a Phase 1b first-in-human study and signed a multi-year anti-aging and cancer research collaboration with Spanish universities.

What are the key Q3 2025/26 financial results for Propanc Biopharma (PPCB)?

Propanc reported total assets of $14.33 million and quarter-end cash of $443,702. According to Propanc, liabilities fell by $2.10 million, convertible notes declined to $55,000 from $538,000, and net cash from financing activities reached approximately $4.47 million.

What is the size and structure of Propanc Biopharma's $100 million private placement (PPCB)?

Propanc arranged a private placement facility for up to $100 million to fund clinical development. According to Propanc, it received an initial $1 million for 100 Series C preferred shares and another $1 million upon exercise, plus a subsequent $0.5 million tranche.

How is Propanc Biopharma advancing its PRP Phase 1b first-in-human trial (PPCB)?

Propanc is preparing PRP for a Phase 1b first-in-human study in advanced solid tumor patients. According to Propanc, it engaged FyoniBio for a pharmacokinetics assay, is discussing GMP manufacturing and CRO support, and is preparing a Clinical Trial Application for submission later this year.

What does Propanc Biopharma's collaboration with the Universities of Jaén and Granada involve (PPCB)?

The collaboration focuses on anti-aging and cancer research using senescence-modulating compounds. According to Propanc, the multi-year agreement supports experiments backing fibrosis and cancer patent applications and explores proenzymes in cancer, cell rejuvenation, and age-related chronic diseases such as fibrosis.

How will Propanc Biopharma's new financing support PRP and Rec-PRP development for PPCB investors?

The financing facility is expected to fund planned R&D for PRP and Rec-PRP. According to Propanc, ongoing access to this up-to-$100 million private placement should support clinical progression and related research activities, potentially helping advance programs targeting cancer and age-related chronic conditions.