$IX Biopharma(42C.SI)$ 0.8 Target Price.

--iX Biopharma Ltd(42C) Growth Catalysts--

Shift towards commercialisation of WaferiX subligual delivery of drugs could bump up revenue by as much as 250% in FY-2026, backed by planned capacity expansion.

Out-licensing of the sublingual ketamine wafer, Wafermine, for Phase 3 development will be a major catalyst and expected to turn iX Biopharma profitable in long-term. 

Specialty pharmaceutical and nutraceutical drugs will benefit from the planned six-fold increase in production capacity to meet the expected surge in demand.

Investment Merits

Out-licensing world's first sublingual ketamine formula, Wafermine, for Phase 3 development is a near-term catalyst.

Since the completion of its end-of-Phase 2 meeting with the US Food and Drugs Administration (FDA), iX Biopharma has been talking to potential out-licensing partners to undertake Phase 3 development trials for acute moderate to severe pain. Successful out-licensing agreements are expected to generate licensing fees for the company, including upfront licensing fees. This is expected to turn iX Biopharma profitable in long-term. 

Ramp-up of pharmaceutical and nutraceutical sales expected with capacity expansion in FY26-28.

Since its successful development of various specialty pharmaceutical and nutraceutical drugs, iX Biopharma has begun commercialising them. It has planned a six-fold increase in production capacity to cater to anticipated demand growth of 252% for its products. This should support sales growth of 270% YoY in FY2026 till 2028.

WaferiX technology offers ample potential for future drug development.

Potential for incorporating WaferiX in off-patent drugs opens opportunities to iX Biopharma for future drug development, given the advantages for the WaferiX technology to be incorporated with various pharmaceutical drugs. When WaferiX is incorporated in a drug with tested and proven clinical effects, the result is a new product with patented intellectual property. This is thanks to its unique formulation which has identical active drug components as traditional formulations.

WaferiX – The Technology

WaferiX is the company's patented sublingual delivery system, which allows for the delivery of active drug compounds through a person's rich supply of blood vessels under the tongue. This promotes rapid absorption of the active compounds in the bloodstream. Drugs that are delivered sublingually avoid challenges faced by drugs that are delivered intravenously or orally (Figure 1).

Drugs that are delivered intravenously can get into the human system the fastest. However, they are invasive and often require medical expertise for proper administration, which requires patients to be in a medical facility to receive the drugs. This results in greater inconvenience and higher costs.

While orally-ingested drugs are more convenient and inexpensive, certain active compounds are less effective as the drugs first have to pass through the digestive system. This results in slower and lower absorption as active compounds have to be broken down (i.e. low bioavailability).

In contrast, sublingual drugs are administered directly under the tongue. This offers convenience as well as higher bioavailability of the drugs. These two features are especially important for drugs that require a quick onset of action, such as for pain management.

The patents granted to iX Biopharma's WaferiX formulation testifies to the uniqueness of its technology as well as WaferiX's efficacy in facilitating the sublingual delivery of drugs. This differentiates WaferiX from other sublingual formulations in the market. Apart from its patented formulation, WaferiX’s proprietary freeze-drying production procedure also confers intellectual-property protection for the technology, further enhancing its appeal.

Business Model

iX Biopharma is primarily a drug developer. It undertakes intensive research and development to incorporate its patented WaferiX in various pharmaceutical drugs. It also operates its own manufacturing and testing facility so as to retain proprietary production procedures. Products are sold to markets such as Australia, China and Singapore through various channels.

It sells its specialty pharmaceutical products in Australia as both registered medicines (Wafesil and Silcap) and unregistered medicine (Wafermine and BnoX) under Schedule 5A of Australia TGA. This schedule stipulates that therapeutic goods may be supplied to hospitals and clinics and bypass extensive developmental procedures, provided the drugs are manufactured in Australia and there are no listed or registered products in the market that are substantially similar.

The company's range of nutraceutical products are sold directly in Australia through retail channels and in China and Singapore on e-commerce platforms, Tmall Global and JD Worldwide (Figure 2).

Out-licensing*: iX Biopharma is pursuing an out-licensing model for its products to penetrate more markets. Out-licensing will allow iX Biopharma to tap the expertise of its licensing partners throughout the developmental and commercialisation phases of a drug, thereby reducing costs and other associated risks.

An out-licensing deal will entail permission to use its trademarks, patents or technology under conditions spelt out in the deal. In return, the licensor will receive recurring milestone payments and royalty payments.

iX Biopharma has inked an out-licensing deal for Wafesil with China-listed Yiling Pharmaceutical. Containing the active compound of sildenafil, Wafesil is a sublingual wafer used for treating MED. Yiling Pharmaceutical will have the rights to sell Wafesil post-product registration in China, while bearing the costs to bring the product to market.

iX Biopharma is also pursuing an out-licensing deal for Wafermine, its sublingual ketamine, for Phase 3 clinical development to treat acute moderate to severe pain. Due to a global need for effective non-opioid treatment of pain, a licensing deal for Wafermine, which will be the world's first ketamine drug for pain is expected to dwarf its Wafesil out-licensing deal in licensing fees.

Business Segments

Specialty Pharmaceuticals: iX Biopharma manages five products under its specialty pharmaceuticals (Figure 3), targeted at the treatment of pain and MED as WaferiX is able to address the needs of patients conveniently with its quick onset of effects and other conditions with its medicinal cannabis product (see Appendix A for details).

Nutraceuticals: The company launched its nutraceuticals portfolio which consists of health supplements marketed under Entity Health. Unlike traditional supplements which focus on specific ingredients such as vitamins or trace minerals, Entity nutraceutical products are formulated with the treatment of specific conditions in mind. They also benefit from the incorporation of WaferiX which provides for higher bioavailability than traditional health supplements (see Appendix A).

Investment Thesis

i. Out-licensing of Wafermine for Phase 3 clinical trials offers potential for multi-million-dollar licensing fees.

iX Biopharma successfully completed end-of-Phase 2 meetings with the US FDA for Wafermine. It is pursuing an out-licensing agreement to see through Phase 3 studies and commercialise Wafermine.

iX Biopharma is prospecting potential out-licensing partners. A successful deal will see the company license out the right to develop and sell Wafermine to other markets in return for licensing fees. Typically, fees include upfront and milestone fees. In the case of Wafermine, its fee schedule will include payments at several developmental milestones before commercialisation. Upon commercialisation, the company is also expected to receive royalty fees from sales plus additional payments upon certain sales milestones reached by its licence partners.

The company is currently in talks with prospective partners for an out-licensing deal. The expected cost of the Phase 3 development of Wafermine is US$25million. It's estimate that any out-licensing deal could be worth multiple times the cost of US$25million, staggered over the entirety of the licensing agreement.

In addition, Wafermine is ready for Phase 2 clinical trials for the treatment of depression. This may boost the valuation of any deal with out-licensing partners should Wafermine be out-licensed for the development of both treatments.

iX Biopharmax revenue grew 47% y-o-y  as it shifted towards commercialisation of its products. It launched Entity flagship stores on two of China largest e-commerce platforms, JD Worldwide and Tmall Global. Its nutraceutical products, LumeniX and RestoriX, were sold out in less than three weeks of launch. Xativa, the first sublingual medicinal cannabis wafer in Australia as an unregistered medicine, also met with strong demand, with its initial production run selling out shortly after its launch.

iii. Clinical experience of working with drugs under development in Australia to accelerate commercialisation.

Many of the drugs that are in the development stage are already being supplied to the Australian market via Schedule 5A of its TGR. Under the regulation, drugs that are manufactured in Australia may be supplied to hospitals as unregistered medicine as long as there are no comparable substitutes in the market. This has allowed iX Biopharma to gather sufficient clinical evidence on the effects of its pharmaceutical drugs under development, including Wafermine and BnoX.

iX Biopharma is pursuing an out-licensing agreement to undertake Phase 3 development of Wafermine for the treatment of acute pain, while also ready for Phase 2 developmental studies for the treatment of depression. If it out-licenses the study of Wafermine concurrently for depression and acute pain, we see the potential for boosting the valuation of any out-licensing deal for Wafermine.

The company sildenafil wafer, Wafesil, is used for the treatment of MED. This has been out-licensed to Chinese pharmaceutical company, Yiling Pharmaceutical, for distribution in China. It is also being registered in the EU for sale and registration outcome is expected by 2H21. The product is pending registration in China and all costs to bring Wafesil to commercialisation in China will be borne by Yiling Pharmaceutical. iX Biopharma will only be responsible for manufacturing the drug after commercialisation.

iv. Novelty in WaferiX technology offers potential for future drug development.

Apart from increased bioavailability when WaferiX is incorporated with drugs (Figure 6), WaferiX possesses high potency for application to active compounds in other drugs. As such, we see ample opportunities for iX Biopharma to incorporate WaferiX in off-patent drugs for the creation of new products in the market. Development risks and costs could be lowered as their active ingredient would have been well-studied for previous formulations.

Apart from WaferiX's formulation, the company proprietary manufacturing procedures also confer intellectual-property protection. Patents that continue to be granted across the globe for this technology testifies to its novelty. Together with its potency for application in other pharmaceutical drugs, we believe the WaferiX technology will underpin income generation from future drugs development.

Financial Highlights and Forecasts

Revenue: Between FY18 and FY20, revenue grew at a CAGR of 100%. 4Q20 revenue of S$0.56mn accounted for 57% of FY20 revenue. As the company continues to push towards commercialisation, we forecast revenue of S$3.47mn annually. This would be supported by a six-fold increase in production capacity by Q4-2026 and further expansion in FY-2027.

As iX Biopharma begins to ramp up production capacity for commercialisation, its gross margins have improved by around 20% annually.

FY-2026 margins are forecast at 40% to reflect the installation of additional freeze dryers, which would add 500% to production capacity and improve economies of scale. As operations stabilise, we expect margins to further improve to 69% in FY-2027, which is on the conservative side in an industry whose margins hover between 80 – 85%.