PolyPid (PYPD) Earnings Call zum 2. Quartal 2026: Prioritäre Prüfung für D-PLEX100 und Azurity-Deal

Wichtigste Erkenntnisse

• Die FDA hat PolyPids Zulassungsantrag (NDA) für D-PLEX100 am 27. Juli 2026 angenommen, keine Mängel bei der Antragsprüfung festgestellt und eine vorrangige Prüfung (Priority Review) gewährt. Das PDUFA-Zieldatum ist der 28. November 2026.
• PolyPid hat eine exklusive Vermarktungsvereinbarung für die USA und Kanada mit Azurity Pharmaceuticals unterzeichnet. Das Unternehmen sicherte sich Vorauszahlungen und kurzfristige Meilensteinzahlungen in Höhe von 30 Millionen US-Dollar und hat Anspruch auf weitere Meilensteinzahlungen von über 290 Millionen US-Dollar.
• Die Vereinbarung sieht für PolyPid zudem gestaffelte Lizenzgebühren im mittleren Teen- bis mittleren 20-Prozent-Bereich vor sowie einen vereinbarten Transferpreis für jede an Azurity gelieferte Einheit.
• Der Nettoverlust verringerte sich im zweiten Quartal 2026 auf 7,8 Millionen US-Dollar bzw. 0,35 US-Dollar je Aktie, verglichen mit 10,0 Millionen US-Dollar bzw. 0,78 US-Dollar je Aktie im zweiten Quartal 2025.
• Das Management geht davon aus, dass die vorhandenen liquiden Mittel, die Erlöse aus der Vermarktungsvereinbarung und potenzielle künftige Zuflüsse den Geschäftsbetrieb bis ins Jahr 2028 finanzieren werden. Laut PolyPid besteht kein unmittelbarer Finanzierungsbedarf.
• PolyPid plant, im dritten Quartal 2026 einen Zulassungsantrag für D-PLEX100 bei der Europäischen Arzneimittel-Agentur einzureichen. Das Management rechnet vorbehaltlich der Genehmigung mit der US-Markteinführung durch Azurity Anfang 2027.

Wichtigste Finanzdaten

In den ersten sechs Monaten des Jahres 2026 belief sich der Nettoverlust auf 15,6 Millionen US-Dollar, verglichen mit 18,2 Millionen US-Dollar im Vorjahreszeitraum.

Zum 30. Juni 2026 verfügte PolyPid über flüssige Mittel von 6,6 Millionen US-Dollar. Zum 31. Dezember 2025 lagen die flüssigen Mittel und Kurzfristanlagen bei 12,9 Millionen US-Dollar. Nach Quartalsende erhielt das Unternehmen eine Vorauszahlung von 15 Millionen US-Dollar von Azurity sowie weitere 15 Millionen US-Dollar nach Annahme des NDA durch die FDA.

Im Juni 2025 ausgegebene Optionsscheine im Wert von rund 7,3 Millionen US-Dollar waren weiterhin ausstehend und laufen im Juni 2027 ab.

Geschäfts- und operative Entwicklung

D-PLEX100 befindet sich in der FDA-Prüfung zur Vorbeugung von chirurgischen Wundinfektionen bei Patienten, die sich einer kolorektalen Operation im Bauchraum unterziehen. Durch die vorrangige Prüfung (Priority Review) verkürzte sich der Prüfzeitraum laut Management von den standardmäßigen 10 Monaten auf sechs Monate.

PolyPid bereitet seine israelische Produktionsstätte auf eine Inspektion vor der Zulassung (Pre-Approval Inspection) durch die FDA vor. Die Anlage hat vier aufeinanderfolgende GMP-Inspektionen bestanden, zuletzt im September 2025 durch das israelische Gesundheitsministerium. Das Management verwies zudem auf die Due-Diligence-Prüfung von Partnern, externe Berater sowie mehrere Testinspektionen als Beleg für die Inspektionsbereitschaft.

Im Rahmen der Vereinbarung mit Azurity behält PolyPid die weltweite Fertigungsverantwortung und die globale Regulierungsstrategie. Azurity wird die kommerziellen Aktivitäten in den USA und Kanada leiten, darunter den Ausbau des Vertriebsteams, die Planung für Großkunden, Medical Affairs, die Vertragsgestaltung sowie die Vorbereitung der Apothekenkanäle.

Azurity verfügt in den USA über mehr als 200 Mitarbeiter im Vertriebsbereich sowie über Beziehungen zu mehr als 1.700 Krankenhäusern und akademischen Einrichtungen. Laut Management wird der Marktzugang schrittweise von Krankenhaus zu Krankenhaus und von integriertem Versorgungsnetzwerk zu integriertem Versorgungsnetzwerk erfolgen.

Die Partnerschaft umfasst ein von Azurity finanziertes gemeinsames Entwicklungskonzept für eine potenzielle Indikationserweiterung von D-PLEX100. Das Management nannte Herzeingriffe (insbesondere CABG), orthopädische Eingriffe (einschließlich Hüft- und Knieoperationen) sowie Mastektomie und Brustrekonstruktion als vorrangige Bereiche, die geprüft werden.

PolyPid behält zudem die vollständigen Rechte an seiner Kynatrix-Technologie. Das Unternehmen prüft Behandlungsanwendungen, darunter ein langwirksames Programm für Stoffwechselerkrankungen, nannte jedoch keine konkreten Zeitpläne für die Entwicklung.

Prognose des Managements

Das Management geht davon aus, dass die aktuellen liquiden Mittel von PolyPid, die Erlöse aus der Azurity-Vereinbarung und potenzielle künftige Zuflüsse den Geschäftsbetrieb bis ins Jahr 2028 und über mehrere potenzielle Meilensteine hinweg finanzieren werden.

Zu den vom Management genannten wichtigsten Meilensteinen gehören:

• FDA-Inspektion der Produktionsstätte von PolyPid vor der Zulassung.
• PDUFA-Zieldatum für D-PLEX100 am 28. November 2026.
• Geplante EMA-Einreichung im dritten Quartal 2026 im Rahmen des zentralisierten Verfahrens.
• Erwartete kommerzielle US-Markteinführung durch Azurity Anfang 2027, vorbehaltlich der behördlichen Genehmigung.

PolyPid rechnet damit, Umsatzerlöse aus der Produktlieferung zu verbuchen, wenn Einheiten von D-PLEX100 im Rahmen der vereinbarten Verrechnungspreisregelung an Azurity verkauft werden. Lizenzgebühren und Meilensteinerlöse werden verbucht, wenn die entsprechenden Ereignisse eintreten.

Risiken und Beobachtungspunkte

D-PLEX100 befindet sich weiterhin in der FDA-Prüfung und steht vor einer Fertigungsinspektion vor der Zulassung. Das Management nannte kein konkretes Inspektionsdatum, erklärte jedoch, dass die Kommunikation mit der FDA Angelegenheiten im Zusammenhang mit erwarteten Audits umfasste.

Die kommerzielle Akzeptanz wird voraussichtlich schrittweise erfolgen. Zu den frühen Indikatoren für den Starterfolg gehören die Aufnahme in Arzneimittellisten von Krankenhäusern, Überprüfungen durch Arzneimittelkommissionen, Pilotprogramme, die Nutzung durch Ärzte, Fortschritte bei der Kostenerstattung und der potenzielle Status für Sonderentgelte im Rahmen des New Technology Add-on Payment (NTAP).

Der geplante europäische Antrag unterliegt ebenfalls der behördlichen Prüfung. Laut Management führten die Gespräche mit dem Berichterstatter (Rapporteur) und dem Ko-Berichterstatter (Co-Rapporteur) zu keinen Problemen, die zusätzliche Daten oder Änderungen erfordern würden, welche die für das dritte Quartal 2026 geplante Einreichung verzögern könnten.

Highlights der Analysten-Fragerunde

• FDA-Inspektion: Das Management lehnte es ab, ein konkretes Datum zu nennen, bestätigte jedoch die laufende Kommunikation mit der FDA bezüglich der während der NDA-Prüfung erwarteten Audits.
• Due Diligence der Produktion: Azurity und andere potenzielle Partner führten Vor-Ort-Prüfungen der israelischen Anlage von PolyPid, der CMC-Prozesse und der Kapazitäten für die Fertigung im kommerziellen Maßstab durch.
• Vorbereitung der Markteinführung: Azurity hat die Marktforschung, die Preisgestaltung, die Einbindung von Meinungsbildnern, den Marktzugang und die Vertragsgestaltung übernommen. Laut Management sind die Marketing- und Vertragsteams bereits vor Ort.
• NTAP-Verfahren: Laut Management benötigt D-PLEX100 vor der Einreichung eines NTAP-Antrags keine Zulassung; es muss sich lediglich in der Prüfung durch die FDA befinden. Azurity arbeitet auf die Frist im Oktober für das nächste Geschäftsjahr der Regierung hin.
• Markteinführungskennzahlen: PolyPid plant die Überwachung von Krankenhausgenehmigungen, Prüfungen durch P&T-Ausschüsse, Pilotprogrammen, der Nutzung durch Ärzte, Erstattungsfortschritten und vertraglichen Mindestmengen im Rahmen der Azurity-Vereinbarung.
• Europäischer Zulassungsantrag: Das Management erklärte, die Sitzungen im Zusammenhang mit der EMA seien produktiv gewesen und hätten nicht zu Forderungen nach wesentlichen zusätzlichen Daten geführt, die das Ziel einer Einreichung im dritten Quartal 2026 verzögern würden.

Vollständiges Transkript der Telefonkonferenz zu den Ergebnissen

Vollständiges Transkript der Telefonkonferenz

Ausführungen des Managements

Operator

Greetings, and welcome to the PolyPid's Second Quarter 2026 Conference Call. As a reminder, this call is recorded.

And I would now like to introduce your host for today's conference, Yehuda Leibler, from Arx Investor Relations. Mr. Liebler, you may begin.

Yehuda Leibler

Thank you, operator, and thank you all for joining PolyPid's Second Quarter 2026 Earnings Conference Call.

Joining me on the call today will be Dikla Czaczkes Akselbrad, Chief Executive Officer of PolyPid; Jonny Missulawin, PolyPid's Chief Financial Officer; and Ori Warshavsky, Chief Operating Officer, U.S., of PolyPid.

Earlier today, PolyPid released its financial results for the 3 and 6 months ended June 30, 2026. A copy of the press release is available on the Investors section of the company's website at www.polypid.com.

I'd like to remind you all that on this call, management will make forward-looking statements within the meaning of the federal securities laws. For example, management is making forward-looking statements when it's discussing the company's exclusive commercialization partnership with Azurity Pharmaceuticals for the United States and Canada.

These forward-looking statements include the partnership's economic structure, including the potential milestone payments, tiered royalties and transfer price, the joint development activities and label expansion program contemplated under the agreement, the expected timing and progress towards potential U.S. Food and Drug Administration or FDA approval of D-PLEX100, including the assigned Prescription Drug User Fee Act or PDUFA goal date and the FDA's grant of Priority Review.

Additional forward-looking statements include the company's engagements with the European Medicines Agency, including meetings with the Rapporteur and Co- Rapporteur regarding the planned Marketing Authorization Application, or MAA, and the anticipated timing thereof, the expected commercial launch of D-PLEX100 by Azurity in the United States in early 2027.

Further forward-looking statements include the company's manufacturing readiness and preparation for the FDA pre-approval inspection, the potential clinical and economic value of D-PLEX100, the company's Kynatrix technology and additional pipeline opportunities, growth drivers and the expectation that the company's existing cash resources will be sufficient to fund operations into 2028 and through several significant upcoming potential milestones.

Forward-looking statements are subject to numerous risks and uncertainties, many of which are beyond the company's control, including the risks described from time to time in the company's Securities and Exchange Commission filings. Accordingly, you should not place undue reliance on these statements.

I encourage you to review the company's filings with the SEC, including the company's annual report on Form 20-F filed on February 25, 2026.

PolyPid disclaims any intention or obligation, except as required by law, to update or revise any forward-looking statements. This conference call contains time-sensitive information and speaks only as of the live broadcast today, August 12, 2026.

With that, it's my pleasure to turn the call over to Dikla Czaczkes Akselbrad, the CEO of PolyPid. Dikla?

Dikla Akselbrad

Thank you, Yehuda. And thank you all for joining us today.

The second quarter of 2026 was a defining quarter for PolyPid. During and shortly after the quarter, we accomplished two transformative milestones that together fundamentally reshaped the profile of our company: first, the FDA's acceptance for filing of our new drug application, or NDA, for D-PLEX100 with Priority Review; and second, the signing of an exclusive commercialization partnership with Azurity Pharmaceuticals for the United States and Canada.

Starting with regulatory progress. During the second quarter, we completed the NDA submission for D-PLEX100 for the prevention of surgical site infection, or SSI, in patients undergoing abdominal colorectal surgery.

Subsequent to quarter end on July 27, 2026, the FDA formally accepted our NDA for filing. This acceptance came ahead of our own internal timeline, reflecting what we see as the strength of the underlying submission package and the collaborative interactions we had with the agency during and prior to filing. Importantly, in the acceptance itself, the FDA identified no filing review issues in our submission. We view this as a meaningful positive signal.

In parallel with the acceptance, the FDA granted the NDA of D-PLEX100 a Priority Review. This is a designation the agency reserves for drug candidate that in its judgment has the potential to represent a significant improvement in the safety or effectiveness of the treatment, diagnosis or prevention of serious conditions. Practically, Priority Review shortens the standard review period from 10 months to 6 months, and it sets our PDUFA goal date to November 28, 2026.

Taken together and ahead of schedule acceptance, no filing review issues, and the grant of Priority Review, represent three outcomes that we believe form a robust starting point to the NDA review process and reflect the strength of the clinical and regulatory foundations we have built with D-PLEX100 over the last several years.

Turning to our commercial partnership. On July 17, 2026, we entered into an exclusive commercialization agreement with Azurity Pharmaceuticals for D-PLEX100 in the United States and Canada. We are very pleased with this partnership. The selection of Azurity reflects not only its proven commercial capabilities, but also its reputation as a long-term strategic partner capable of unlocking the full value of differentiated specialty pharmaceutical assets.

Ori will provide some color in a moment on why we are so excited about having Azurity as our commercial partner, including the competitive business development process behind our selection. At a high level, we view the economic structure of this partnership as exceptionally strong for a commercialization deal at this stage.

We already secured a total of $30 million in upfront and near-term milestone payments. In addition, we are eligible to receive over $290 million in additional regulatory launch and sales milestones. I want to be clear that these milestones are structured around specific corporate, regulatory and commercial events that align directly with the D-PLEX100 operational and launch plans. We believe that these milestones are achievable during the term of the agreement and are not a stacked structure designed to inflate the headline number.

In addition to this milestone payment, PolyPid is entitled to tiered royalties on Azurity sales in the U.S. and Canada, ranging from mid-teens to mid-20s percentages. PolyPid will manufacture and supply the product, generating an additional agreed transfer price on every unit supplied to Azurity. Unlike most licensing deals in our industry where the licensor participates only through royalties, we made a strategic choice several years ago to retain manufacturing globally. That choice now positions PolyPid to potentially capture a meaningful share of the ultimate end product economics.

I want to make one broader point about the deal economics. A partnership structure like this one with multiple components can be complex. And we recognize that some observers may focus on any single component in isolation. Taken as a whole, however, we believe the combination of secured upfront event-driven milestones, tiered royalties, agreed transfer price on every manufactured unit and an Azurity-funded label expansion pathway, represent unusually strong economics for a company at our stage in commercialization partnership of this kind.

Jonny will walk you through this architecture and its balance sheet implications in more detail shortly.

In preparation for the upcoming launch, we continue to advance our manufacturing and inspection preparations. Our facility has already passed four consecutive successful good manufacturing practice, or GMP inspections, including the most recent one by the Israeli Ministry of Health in September 2025.

During the commercial evaluation process, prospective commercial partners conducted on-site diligence at our site in Israel, providing external validation of our manufacturing readiness posture. Our team continues to work closely with experienced external consultants and have conducted multiple mock inspections in preparation for the FDA pre-approval inspection that will follow. We are entering this process from a position of strength and are highly focused on getting it right at first time.

Turning to Europe. During the second quarter, we held meetings with the Rapporteur and Co- Rapporteur, the European regulatory authorities designated to lead the assessment of our planned MAA for D-PLEX100. These meetings were productive and positive, and we currently plan to submit the MAA to the European Medicine Agency in the third quarter of this year under the Centralized Procedure, which, if approved, will enable the product to be marketed across all EU member states.

Before I hand the call over to Ori, I want to briefly summarize the key upcoming milestones that investors should be tracking over the coming quarters: first, the FDA pre-approval inspection of our manufacturing facility following NDA acceptance; second, our goal date under PDUFA of November 28, 2026; third, our planned MAA submission to the European Medicine Agency in the third quarter of this year; and fourth, the expected commercial launch of D-PLEX100 by Azurity in the United States in early 2027.

With that, I will now turn the call over to Ori. Ori?

Ori Warshavsky

Thank you, Dikla. I would like to spend a few minutes on Azurity on the joint launch preparation now underway, on the progress we have made around D-PLEX100 this quarter, and finally, on our broader Kynatrix technology opportunities beyond the Azurity partnership.

Beginning with Azurity. The partnership process that we have discussed on prior quarterly calls many times was focused on identifying a partner with the capabilities, focus and infrastructure to make D-PLEX100 a successful commercial trial. This was a rigorous process, and importantly, it was a highly competitive one. We engaged with multiple potential commercial partners, all with robust hospital infrastructure, and several of those discussions progressed to very advanced stages.

In our judgment, Azurity emerged as the partner best positioned to lead the U.S. and Canada launch of D-PLEX100. Azurity is an established specialty pharmaceutical company with a first-in-class commercial model and a portfolio of over 50 medicines spanning 10 therapeutic areas. Azurity is backed by QHP Capital, a health care-focused private equity investor.

Beyond capital, we believe several elements of Azurity's track record position them uniquely well to commercialize D-PLEX100. Azurity has an antibiotic on the market which gives them established credibility with infectious disease specialist. The core audience for D-PLEX100, Azurity also markets bowel prep products in the exact same colorectal surgery call point that D-PLEX100 initially target, giving them existing relationship with the same prescribers.

And with more than 10 additional hospital administered products already on the market, Azurity brings the GPO infrastructure, hospital contracting expertise and institutional relationships that reach over 1,700 leading hospitals and academic institutions in the U.S., a footprint that takes years to build.

With over 200 U.S. commercial-facing colleagues, just under 1,000 employees worldwide and a specialty pharma orientation across hospital and surgical channels, we believe Azurity is uniquely positioned to reach the surgeons, infection specialists, hospital pharmacy directors and value analysis committees who will drive D-PLEX100 adoption. Their dedicated hospital-facing and surgical-facing sales capabilities align directly with the way D-PLEX100 will be prescribed and administered in a way that few counterparties in our process could match. In short, Azurity brings the scale, focus and execution capability that we believe D-PLEX100 needs at launch.

Beyond the initial license territories, Azurity has established commercial operations and partnerships spanning more than 50 countries. While the current agreement is focused on the U.S. and Canada, Azurity's international infrastructure and experience launching specialty medicines creates strategic optionality when additional geographic opportunities are pursued in the future.

The joint work between our teams to prepare for launch is now well underway. We have established joint forums to align on medical, regulatory and commercial preparation. Azurity is leading on-the-ground commercial activities, including sales force build-out, national account planning, medical affairs and pharmacy channel work, while PolyPid retains responsibility for global manufacturing and global regulatory strategy. This division of labor plays to each part of the strength.

The partnership also includes a joint development framework funded by Azurity to pursue label expansion opportunities of D-PLEX100 in additional indications beyond the abdominal indication. D-PLEX100's mechanism and platform supports broader use across other SSI relevant surgical settings and Azurity's willingness to fund that expansion work is a strong signal of the commercial opportunity.

Finally, I want to spend a moment on how we think about PolyPid's growth drivers in the near and midterm. The first growth driver is D-PLEX100 label expansion to additional surgical site infection indications beyond prevention of SSI in abdominal surgery, significantly expanding the total addressable market to other areas of unmet need such as C-section surgery and joint replacement. This label expansion will be funded by Azurity through the joint development framework.

The second growth driver is expanding D-PLEX100 to other territories outside the U.S. and Canada, which are under Azurity partnership.

And finally, the third growth driver is the expansion of the pipeline under our Kynatrix technology, over which PolyPid retains full ownership and which is where we see even broader significant long-term potential as we grow as a company.

In terms of our pipeline, we are now exploring exciting areas that go beyond prevention and into treatment applications. Our long-acting metabolic program is one such area we have previously discussed. We are also exploring high-value areas where we believe we can advance programs relatively quickly to the clinic by leveraging the clinical, manufacturing and safety foundation we have already built for D-PLEX100.

In many of these cases, we believe that the mechanistic and CMC platform we built around D-PLEX100 can materially compress the path to meaningful clinical stages for programs that would otherwise require years of de novo formulation and preclinical work. We look forward to sharing more on specific pipeline products as those plans evolve.

With that, I will now turn the call over to Jonny to review our financial performance for the quarter. Jonny?

Jonny Missulawin

Thank you, Ori. I will now walk through our financial results for the second quarter ended June 30, 2026, and highlight the material developments impacting our balance sheet.

Starting with the Azurity partnership, as Dikla noted, we have already secured $30 million in aggregate upfront and near-term milestones from our partnership with Azurity and are eligible for over $290 million in additional regulatory, launch and sale milestones.

On top of these payments following commercial launch, we expect to generate two additional ongoing revenue streams: tiered royalties on Azurity sales in the United States and Canada in the range from mid-teens to mid-20s percentages; and a transfer price on every unit we manufacture and supply to Azurity. The label expansion program under the joint development agreement is funded by Azurity and expands the addressable base for both revenue streams over time without requiring incremental PolyPid capital.

Turning to our income statement for the quarter. Research and development expenses for the second quarter of 2026 were $6.1 million compared to $6.2 million in the second quarter of 2025.

R&D activity in the second quarter of 2026 primarily reflects ongoing NDA-related activities and continued commercial readiness preparation.

General and administrative expenses were $1.3 million compared to $2.5 million in the prior year period. The decrease was primarily due to the decrease of noncash expenses related to performance-based options following the positive Phase III SHIELD II topline results, which triggered the vesting of those options.

Marketing and business development expenses were $0.5 million compared to $0.7 million in the prior year period.

Net loss for the second quarter of 2026 was $7.8 million or $0.35 per share compared to a net loss of $10 million or $0.78 per share in the second quarter of 2025. For the first 6 months of 2026, net loss was $15.6 million compared to $18.2 million in the first 6 months of 2025.

Turning to the balance sheet. As of June 30, 2026, PolyPid had $6.6 million in cash and cash equivalents compared to $12.9 million of cash, cash equivalents and short-term deposits at December 31, 2025.

Subsequent to quarter end, our capital position has been further strengthened by $15 million upfront payment from Azurity at signing and the additional $15 million as a result of the FDA acceptance of the NDA filing.

Looking at our remaining warrant position, the only warrants outstanding are the warrants issued in June 2025, of which approximately $7.3 million remain outstanding with an expiration date in June 2027. These warrants are by their terms stapled to the shares issued in June 2025, meaning that if a holder sells or transfer those shares prior to exercise of the new warrants, the corresponding new warrants are forfeited. We view this structure as a meaningful alignment mechanism with our long-term shareholder base.

Taken together, we believe this puts the company in a materially stronger financial position today than at any prior point in the D-PLEX100 development journey, while also providing a streamlined and healthier capital structure for PolyPid and our shareholders.

Based on our current plans and assumptions, we expect our existing cash resources, together with the expected proceeds from our recently announced commercialization agreement as well as future potential proceeds will be sufficient to fund operations into 2028 and through several significant upcoming potential milestones. And we do not have immediate financing needs in the near future.

With that, we will now open the call for questions. Operator?

Operator

[Operator Instructions] Your first question comes from Chase Knickerbocker from Craig-Hallum.

Fragen und Antworten

Chase Knickerbocker

Congrats on all the progress here. Maybe just first for me on kind of upcoming expected inspection. Has FDA communicated anything to you as it relates to the potential timing of your pre-approval inspection? And then, as a part of the deal with Azurity, would love to hear the sort of work that went into them getting comfortable on the CMC side, do they -- did they do a fairly strenuous kind of mock audit kind of series as a part of the due diligence?

Dikla Akselbrad

So with regards to our communication with the FDA, since we submitted the NDA, we had several back-and-forth communication in different aspects, including things that are relating to the different audits that are expected as part of the NDA review. I don't think it makes sense to go into more detail, but I could say that we see the process as very effective and efficient, as you would expect from a Priority Review, which leaves both the agency and the sponsor a relatively short time to review everything.

So we are super cooperative with any request that is coming from the FDA to meet the timeline. And I wouldn't go into specific dates on specific request. But as I said, we had several communication from the time that we have submitted, including communication relating to the different audits that are expected.

With regards to the CMC, that's something we tried to highlight in the formal portion by highlighting both the work that we did with Azurity, but also with other potential partner that we had at the time. And as Ori mentioned, we had on-site due diligence in the Israeli site by the Azurity team and by others that were competing for this asset to see both the facility, the CMC processes, the package, everything that could give a potential partner the comfort that this product will be approved and we as a partner could manufacture on a commercial scale and support the launch of the product.

So from that perspective we are very confident that we had several, you could say, external validation, both from other regulatory inspection that we did, the potential partner including -- partners including Azurity as well as mock inspection that we have performed with external advisers.

Chase Knickerbocker

Got it. And maybe just last for me. I would just like to understand kind of the level of overlap that existing Azurity reps have into that kind of colorectal and general surgeon call point. How many reps are kind of calling on those physicians today in their kind of hospital-focused segment?

And do you have any idea at this stage how many of those 200 customer-facing representatives that you mentioned will have D-PLEX in the bag at launch?

Ori Warshavsky

Yes, I can take some of that. So we can't really break down the Azurity sales team. But they do already call -- as we said, they do already call upon colorectal surgeons and in other areas in the hospital. That's kind of one part of it. The other part is they have a significant buildup to expand the capabilities that they have in preparation for the launch and buildup in the market access piece and the contracting piece and on the medical team. So they are putting a lot of efforts ahead of this launch.

Like I mentioned earlier, they are already in 1,700 hospitals and academic centers. That's their target. Obviously, not all on day 1. There will be a gradual hospital-by-hospital and IDN-by-IDN kind of a stepwise approach, but this is the coverage that they're going for.

Operator

Your next question comes from Jason Butler from Citizens.

Jason Butler

A couple on the Azurity partnership. On the commercial side, obviously, it's only been a short period of time, but what are you already doing with Azurity to get them ready for the launch? You've obviously done a lot of pre-commercial work. What are they now doing to prepare for the D-PLEX100 launch?

And then second, on the development side, how are you thinking about the initial label expansion efforts? And how quickly under this collaboration could additional trials begin for additional indications?

Ori Warshavsky

I'll take the...

Dikla Akselbrad

You take the first -- yes.

Ori Warshavsky

The first piece. So a few points here. First, Azurity has been planning -- we've been in conversation with them for a period of time now, and they -- they've not started -- they haven't filed just 3 weeks ago. They have been thinking about this for a while now. And so they're really hitting the ground running on taking ownership of a lot of these activities.

So we've transferred a lot of the knowledge, studies that were done, market research, pricing, KOLs that were done, assessments of NTAP and so on. So this was handed over, and they have their own plans in place to take and expand. So we know NTAP is coming. That's one thing. We know we're building a network of KOL. The American College of Surgeons Conference is this week, Azurity is there. IDWeek is in a couple of months, Azurity will be there trying to build this network.

And some of the activities that can be done before approval, some of the prior approval, access conversations and after approval, MSLs on the ground, reaching out to PIs and reaching out to KOLs and start kind of discussing and introducing the product. So all these plans are in place. The marketing team is in place. The contracting team is in place. And so that's really -- Like I said, we're not starting at step zero. We're starting at step 4.

Dikla Akselbrad

With regards to the label expansion, the joint development framework work is scoped around D-PLEX100 and additional surgical site infection indication behind the initial abdominal indication, obviously. And we will first need to see with the FDA what will be the final indication. But what I can say is that the indication commonly identified as our top target is consistent with the way Azurity sees it.

So what we have discussed really publicly for years, think about cardiac procedure, specifically CABG, orthopedic, including hip and knee and breast mastectomy and reconstruction. Those are the top indication that we view and Azurity view as a few of the top that should be pursued.

Operator

Your next question comes from the line of Boobalan Pachaiyappan from ROTH Capital Partners.

Boobalan Pachaiyappan

Maybe can you discuss the key KPIs you would use internally to track the D-PLEX100 launch success? Let's say, are you going to track -- obviously, you're going to track formulary events, but ultimately, what are the key KPIs that you wanted to like target, activation of hospitals, surgeon users? Can you elaborate more on that?

Dikla Akselbrad

So there are a couple of things here that will be reviewed. Some of it is coming from looking at the collaboration and the partnership that we have and some of the Azurity commitments that is in the agreement that -- and the minimums that are part of the structure of the agreement. So this is obviously something that we will monitor.

There will be also aspects relating to hospital and specifically within the hospital P&T committees, a number of hospitals that are approving or adding to their -- to the pharmacy the drug. And you should also think about things that are part of a drug like this, things like NTAP, and progress around the reimbursement and the conversation with payers. This is the third compound.

Ori, would you want to add anything?

Ori Warshavsky

[indiscernible] view -- So obviously, as Dikla mentioned, the stepwise approach seeing month by month how many hospitals get -- are added, where P&T reviews are review the product and then if there's pilot studies that are done and doctor's usage. Yes, I think those will be the initial ones to see really how successful, let's say, the first 12 months from launch this will be in the main benchmark.

Boobalan Pachaiyappan

Let's say, the drug is indeed launched in first quarter '27. Can you discuss when would this revenue be recognized?

Dikla Akselbrad

So we indicated that it's early 2027. And we will be recognizing revenue quite immediately because as you probably remember, one of the compounds of the structure of the deal is the pre-negotiated transfer price per vial. So every vial that we will sell we will -- to Azurity, we will recognize revenues there. There will be the second compound on royalties and milestone, and those will be recognized as they come.

Boobalan Pachaiyappan

Okay. Maybe one final question from me. So you indicated that the EMA submission is targeted in third quarter '26. So can you maybe provide us a sense of the receptivity to the clinical package during your dialogue with them? Are there any concerns that they have raised about clinical or statistics for safety and things like that?

Dikla Akselbrad

So it was very -- First, thank you for this question. I think it's very important also when, again, looking at the strength of our regulatory package. We had two meetings during the quarter with the Rapporteur and the Co-Rapporteur. Those meetings are the equivalent to a pre-NDA meeting at the FDA. And the purpose of the meeting was similar to a pre-NDA meeting, to align the requirement, to align the timeline.

For us, it was very productive. We had, I wouldn't say changes, but more -- each regulatory arm has their own sensitive area where they want to see additional or where they put the focus, and this was very helpful for us to accommodate. But you could understand from the timeline of the fact that we met them towards the end of June, and we are submitting the package before the end of this quarter, that nothing there was major that required any additional data or changes to the package that will delay the submission time frame.

Operator

[Operator Instructions] We will take our next question and your question comes from the line of Brandon Folkes from H.C. Wainwright.

Brandon Folkes

Congrats on all the progress. Maybe just two from me. Can you just talk about the earlier PDUFA date and what that does in terms of ability to supply the market or launch date? Do you still expect a 1Q launch?

And then similarly, with the November PDUFA date, any impact on the NTAP process there in terms of when it could come online for D-PLEX100?

Dikla Akselbrad

So first, as you can imagine, since we knew that the product has a breakthrough therapy designation and could be eligible for a Priority Review, we prepared for both scenarios. We prepared for before end of the year approval PDUFA date and early 2027 PDUFA date. So we prepared both in terms of NDA submission, getting ready for all the audits, whether it's the GCP or the GMP, as well as launch.

So from our perspective, having the PDUFA date earlier than anticipated doesn't change anything. And we were very happy with that. I think it again shows the strength of the package and the potential that the product has to improve both the effectiveness and safety of the treatment.

As for the QIDP, there are a couple of things -- in the NTAP, sorry, I said...

Ori Warshavsky

Yes. Let me take that. So the NTAP, first, the product does not need to be approved to submit the NTAP. It just needs to be under review with the FDA. So from that point, we have no issue. And Azurity is working the -- to get the -- to be on the next year's financial year -- governmental financial year, the deadline is October, and this is what Azurity is working towards.

Brandon, anything else?

Operator

As there seems to be no response, this concludes today's question-and-answer session. I will now hand back for closing remarks.

Dikla Akselbrad

Thank you for joining PolyPid's second quarter 2026 earnings conference call. This has been a defining quarter for PolyPid, and we are highly confident in our long-term prospects, especially the potential of D-PLEX100 in the hands of Azurity as our commercial partner in the United States and Canada and the broader Kynatrix technology behind it.

As we look ahead to the November 28 PDUFA goal date and the expected commercial launch of D-PLEX100 in early 2027, we are grateful for our team members, shareholders and all external partners for their commitment to our mission and support in continuing to advance toward our goal of bringing D-PLEX100 to health care providers and patients as quickly as possible.

We look forward to speaking with you again on our next conference call.

Operator

This concludes today's conference call. Thank you for participating. You may now disconnect.