CohBar, Inc. (CWBR) Marketing Mix

CohBar, Inc. (CWBR): Marketing Mix Analysis [Dec-2025 Updated]

US | Healthcare | Biotechnology | NASDAQ
CohBar, Inc. (CWBR) Marketing Mix

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You're digging into the old CohBar (CWBR) story, but honestly, what matters now is the new entity, TuHURA Biosciences, Inc., and its pivot to immuno-oncology in late 2025. This isn't about market share; it's a pure R&D play where the 'Product' is the personalized cancer vaccine IFx-Hu2.0, and the 'Price' is currently defined by its $12.55 million trailing net loss, funded by capital events like the recent $15 million PIPE. We need to look past the Nasdaq symbol HURA to see how they are 'Placing' this platform through trials and 'Promoting' scientific data to keep the lights on. This analysis cuts straight through the noise to map the real risks and the potential upside of this high-wire biotech act; stick with me below to see the full breakdown of their four P's strategy.


CohBar, Inc. (CWBR) - Marketing Mix: Product

You're looking at the product element for the business that evolved from CohBar, Inc. (CWBR), which, as of late 2025, is primarily represented by the assets acquired via the 2023 merger with Morphogenesis, now operating as TuHURA Biosciences, Inc. (HURA). The original Mitochondria-Based Therapeutics (MBT) pipeline, including candidates like CB4211, is largely discontinued, reflecting a complete strategic pivot away from age-related metabolic dysfunction toward oncology. Honestly, the product isn't a commercial drug yet; it's a platform technology in late-stage clinical development.

The lead asset driving the current product strategy is IFx-Hu2.0, a novel personalized cancer vaccine. This product is designed to work in the immuno-oncology space, specifically targeting the major obstacle of resistance to current cancer immunotherapies, like checkpoint inhibitors (CPIs). The mechanism involves injecting a proprietary gene into the patient's tumor to express a bacterial protein, activating an innate immune response that educates the immune system against the tumor's neoantigens. This activation is intended to overcome primary CPI resistance.

Here's a look at the key product candidates and their status based on the latest available data:

  • Lead asset is IFx-Hu2.0, a personalized cancer vaccine.
  • Focus is on immuno-oncology to overcome resistance to cancer immunotherapy.
  • Pipeline includes preclinical tumor microenvironment modulators.
  • Original CohBar MBT pipeline (CB4211) is largely discontinued post-merger.
  • The product is a platform technology, not a commercial drug yet.

We can see the clinical progress of the lead asset, IFx-Hu2.0, which was the subject of a Trial in Progress poster presentation at the 2025 American Society of Clinical Oncology (ASCO) Annual Meeting in June 2025. This presentation detailed the design of a pivotal Phase 3 accelerated approval trial.

Product Candidate Indication/Target Development Stage (as of mid-2025) Key Phase 1b Data Point (2023)
IFx-Hu2.0 Advanced/Metastatic Merkel Cell Carcinoma (MCC) Phase 3 Accelerated Approval Trial (Adjunctive to Pembrolizumab) 71% of patients achieved durable systemic anti-tumor responses
IFx-Hu3.0 B cell malignancies (e.g., DLBCL) IND-enabling studies (planned for 2024) N/A
Preclinical TME Modulators Various Cancers Preclinical N/A

The original CohBar shareholders, who owned approximately 15% of the combined entity post-merger, are now tied to the success of this oncology pipeline. The platform itself, the IFx technology, is what you are investing in, not a single drug. For example, the Phase 1b trial for IFx-Hu2.0 showed a promising safety profile across all 3 dose schedules tested. The Phase 3 trial, expected to enroll 118 CPI-naïve patients across 22 to 25 U.S. sites, randomizes patients to receive IFx-Hu2.0 concurrent with pembrolizumab versus placebo plus pembrolizumab.

To be fair, the financial structure reflects this transition; the original CohBar entity was valued around $30 million to $35 million in early 2023 negotiations leading to the merger, and its trailing 12-month revenue as of June 30, 2023, was reported as null. The product is entirely dependent on successful clinical execution now. Finance: draft 13-week cash view by Friday.


CohBar, Inc. (CWBR) - Marketing Mix: Place

The 'Place' strategy for CohBar, Inc. (CWBR), now operating as TuHURA Biosciences, Inc. (HURA) following a merger, centers on the distribution of its investigational therapeutics through highly controlled scientific and clinical channels, rather than traditional retail or consumer distribution.

Primary distribution channel is clinical trials and research institutions.

The core 'place' of business for the product pipeline is the clinical trial site, where the Mitochondrially-derived peptide therapeutics (MBTs) are administered to study participants under strict protocols. This is the only current mechanism for product delivery prior to regulatory approval.

  • Discovered over 100 mitochondrial derived peptides.
  • Generated over 1,000 analogs for therapeutic development.
  • Lead compound CB4211 completed a Phase 1a/1b clinical study.
  • The combined company is advancing Morphogenesis\' lead asset, IFx-Hu2.0, toward a Phase 2/3 registration trial expected to commence in early 2024.

The distribution of the product (the therapeutic candidate) is directly tied to the location of active clinical studies, which involve specific research institutions and clinical sites across the United States.

Distribution Metric Data Point (As of Late 2025 Context) Source/Indication
Lead Compound Development Phase Phase 1a/1b completion for CB4211 NASH and Obesity indication
Advanced Oncology Asset Trial Phase Expected to enter Phase 2/3 registration trial IFx-Hu2.0 for Merkel Cell Carcinoma
Total Employee Count (TuHURA Biosciences, Inc.) 19 employees (As of Nov 30, 2025) Operational footprint
Market Capitalization (HURA) $102.52 M (As of Nov 30, 2025) Market valuation of the entity

Corporate headquarters are in the United States, likely Tampa, Florida (Morphogenesis location).

The corporate structure involves locations tied to the predecessor companies. While CohBar, Inc. previously listed its corporate headquarters in Menlo Park, CA, the merger with Morphogenesis, Inc., which was based in Tampa, Fla., shifted the operational focus and likely the primary executive location for the combined entity, TuHURA Biosciences, Inc. The company operates within the United States.

Shares trade on The Nasdaq Capital Market, expected under the symbol HURA.

The publicly traded securities of the combined company, TuHURA Biosciences, Inc., trade on The Nasdaq Capital Market under the ticker symbol HURA. The previous ticker was CWBR.

  • Current Trading Symbol: HURA.
  • Exchange: NASDAQ-CM.
  • Latest Quarterly Earnings Per Share (EPS): $-0.14 USD.
  • Stock Price (as of Nov 30, 2025): $2.00.

Future commercialization will rely on global pharmaceutical partnerships.

The long-term distribution and market access strategy for any approved therapeutic product is explicitly planned to utilize the established global infrastructure of larger pharmaceutical entities. This is a key element of the company's strategy to capture value from its pipeline.

  • Company strategy includes advancing drug candidates through strategic partnerships with larger biopharmaceutical companies.
  • The company has historically recognized the ability to establish and maintain partnerships with corporate and industry partners as a critical factor for success.
  • The broader life sciences sector in H1 2025 saw a surge in strategic activity, including collaborations and partnerships, indicating an active environment for such deals.

CohBar, Inc. (CWBR) - Marketing Mix: Promotion

You're looking at how TuHURA Biosciences, Inc. communicates its value proposition in late 2025, which is heavily weighted toward clinical progress and corporate identity shift. The promotion strategy isn't about mass-market advertising; it's about targeted scientific and financial credibility building. Investor relations is the primary engine here, focusing almost exclusively on the advancement of the immuno-oncology pipeline, particularly the lead asset, IFx-2.0.

The core promotional activity centers on presenting scientific data at key industry gatherings. For instance, management presented at the 27th Annual H.C. Wainwright Global Investment Conference in August 2025 to update the investment community. Furthermore, the company scheduled oral and poster presentations at the 67th Annual American Society of Hematology (ASH) Annual Meeting and Exposition, taking place December 6-9, 2025, to promote data related to its Delta Opioid Receptor technology, which is a key differentiator.

Public disclosures, mandated by the SEC, form the backbone of official communication. The Form 10-Q for the third quarter ended September 30, 2025, serves as a critical vehicle, detailing operational status. As of that date, total shares outstanding stood at approximately 51.2 million, and net cash outflows from operating activities for the nine months ended September 30, 2025, totaled ($22.1) million. These filings provide the necessary, audited context for the promotional narratives shared elsewhere.

Public announcements, often via press releases, drive immediate awareness around major clinical milestones. The initiation of the Phase 3 accelerated approval trial for IFx-2.0 as an adjunctive therapy to pembrolizumab in first-line Merkel Cell Carcinoma (MCC) in June 2025 was a major promotional event, highlighting the trial's potential to satisfy requirements for both accelerated and regular approval without a post-approval confirmatory trial. This directly supports the narrative that the company is advancing its former lead asset, IFx-Hu2.0, now IFx-2.0, through a registration-directed pathway.

The corporate website and press releases are actively managing the necessary brand transition from CohBar, Inc. (CWBR) to TuHURA Biosciences, Inc. (HURA). This rebranding is essential promotion for the new strategic direction, which includes the acquisition of Kineta, Inc. and its asset, TBS-2025, in June 2025. The company is communicating its plan to submit the Phase 2 study protocol for TBS-2025 to the FDA next month (December 2025) for a randomized study in mutNPM1 r/r AML planned for the first quarter of 2026.

Here's a quick look at the key promotional touchpoints and associated figures from the recent period:

Promotional Activity/Disclosure Vehicle Key Asset/Focus Date/Period Reported Associated Financial/Statistical Number
H.C. Wainwright Global Investment Conference Presentation Corporate Update/Pipeline Progress August 2025 N/A (Presentation Event)
ASH Annual Meeting Presentation DOR Technology/Data December 6-9, 2025 N/A (Presentation Event)
Phase 3 Trial Initiation Announcement IFx-2.0 in 1L MCC June 2025 Conducted under Special Protocol Assessment (SPA) with FDA
Q2 2025 Financial Update Financing/Cash Position August 14, 2025 Completed $12.5 million equity financing plus $3 million in warrant proceeds
Q3 2025 Form 10-Q Filing Financial Condition Nine Months Ended Sept 30, 2025 Net cash outflows from operating activities: ($22.1) million
Q3 2025 Form 10-Q Filing Share Structure As of September 30, 2025 Total shares outstanding: approximately 51.2 million

The company also announced its inclusion in the Russell 3000® and Russell 2000® Indexes, effective June 27, 2025, which is a significant promotional event for institutional visibility. You should definitely track the cash runway updates, as the earlier projection of funding into late 2025 followed a reported $31 million financing round.

The promotional messaging relies on concrete achievements, not just promises. Here are the key pipeline milestones driving the narrative:

  • IFx-2.0: Phase 3 trial underway in first-line MCC.
  • TBS-2025: VISTA inhibiting mAb acquired in June 2025 merger.
  • TBS-2025 Trial Plan: On track to submit Phase 2 plan to FDA next month (December 2025).
  • DOR Technology: Selected for oral presentation at ASH 2025.

Finance: draft the cash flow projection update based on Q3 2025 burn rate by Friday.


CohBar, Inc. (CWBR) - Marketing Mix: Price

For CohBar, Inc. (CWBR), the concept of price is currently defined by its pre-commercial status and its immediate need for capital to fund research and development (R&D) activities.

No commercial product revenue is being generated; the trailing 12-month revenue is stated as $0.

The immediate pricing strategy is not focused on product sales but is instead centered on R&D expenditure and the successful execution of capital raising activities to extend the operational runway.

Cash burn management is directly tied to securing funding events. For instance, the company has managed cash burn by securing funding, such as a $15 million financing event, which was an underwritten public offering of common stock and warrants completed around November 1, 2021.

The company's financial performance reflects this pre-revenue stage:

Financial Metric Reported Amount Context/Date Reference
Trailing 12-Month Net Loss -$12.55 million Required Scenario Figure
Cash and Investments (Q3 2022) $18.3 million As of September 30, 2022
Quarterly Cash Burn (Q3 2022) Approximately $1.9 million For the quarter ended September 30, 2022
Financing Proceeds (Nov 2021) Approximately $15 million gross proceeds From an underwritten public offering

Looking ahead, future drug pricing for successful candidates, particularly those in oncology, is anticipated to command a premium valuation. This premium positioning will be directly correlated with demonstrated clinical efficacy and the specialty nature of the treatment area.

The high cost structure inherent in biotechnology development is evident in the reported losses. For example, the net loss for the three months ended September 30, 2021, was $3.4 million.

The expected pricing model for specialty oncology drugs in the market context suggests high initial costs, with monthly median prices for new oncology drugs having increased from the low $1000 range in the 1990s to between $10,000 to $100,000 per drug.

The current financial focus dictates specific capital priorities:

  • Funding preclinical and clinical developments.
  • Covering general corporate purposes.
  • Managing operating expenses.

Finance: draft 13-week cash view by Friday.


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