Paradigm Biopharmaceuticals Adds CMO With Rheumatology Depth Ahead of Phase 3 Readout

Paradigm Biopharmaceuticals appoints Chief Medical Officer Dr Daniel Furtner — a former CSL and AbbVie executive with 20 years of rheumatology and medical affairs experience — as the fully recruited 538-patient Phase 3 osteoarthritis trial moves into its evidence generation phase ahead of a Q1 2027 top-line readout.
By Josua Ferreira -
  • Dr Daniel Furtner, formerly Senior Director of Medical Affairs (Asia Pacific) at CSL with over 20 years of rheumatology and pharmaceutical leadership experience, joins Paradigm as Chief Medical Officer effective 16 September 2026.
  • Dr Donna Skerrett transitions from CMO to Senior Scientific Advisor, retaining seven years of institutional knowledge about the iPPS program at the company rather than departing.
  • The Phase 3 PARA_OA_012 trial has completed recruitment with 538 participants across 65 sites in four countries, surpassing the original 466-participant target, with an Interim Analysis due September 2026 and top-line results expected Q1 2027.
  • A pro forma cash position of approximately $45 million following a $14 million placement is expected to fund operations through to end of CY2026, covering the interim analysis without a dilutive raise under the current plan.
  • The CMO transition is designed to align medical leadership with the program's shift from trial execution to evidence package assembly and regulatory submission preparation.
Summarise with AI:

Paradigm strengthens medical leadership ahead of Phase 3 readout

Paradigm Biopharmaceuticals has appointed Dr Daniel Furtner as Chief Medical Officer, effective 16 September 2026. Dr Furtner succeeds Dr Donna Skerrett, who transitions to Senior Scientific Advisor, ensuring continuity of expertise as the company advances its clinical evidence package for injectable pentosan polysulfate sodium (iPPS; Zilosul®) and prepares for future regulatory submissions.

Dr Furtner’s credentials and what he brings to Paradigm

Dr Furtner’s background closely aligns with Paradigm’s current development priorities, particularly as the Phase 3 program shifts from recruitment to evidence generation.

Career and qualifications highlights:

  • Over 20 years of leadership experience across life sciences and healthcare
  • Most recently served as Senior Director of Medical Affairs (Asia Pacific) at CSL, based in Melbourne
  • Previously held roles of increasing responsibility at Abbott/AbbVie and Janssen across Europe, Asia and Australia
  • Therapeutic focus spans rheumatology, immunology and joint diseases, mapping directly to Paradigm’s osteoarthritis program
  • Led international clinical studies and educational programs in support of patients, caregivers and nurses
  • Holds a Doctor of Medicine from the Medical University of Vienna; completed residency at Klinik Donaustadt and the Lorenz Böhler Trauma Centre
  • Holds a Master of Business Administration in general management from Danube Business School, Krems, Austria

Paul Rennie, Executive Chairman

“Daniel brings extensive international pharmaceutical experience and deep therapeutic knowledge in rheumatology and joint diseases. His experience in medical affairs and international clinical studies will be valuable as we advance our Phase 3 program and develop the evidence package to support future regulatory submissions. Having Daniel lead our medical strategy, with Donna’s continued scientific support, provides a strong foundation for this next stage.”

Dr Skerrett’s legacy and her continuing role

Dr Skerrett has served as Paradigm’s Chief Medical Officer since September 2019, playing a central role in shaping the company’s clinical and regulatory development strategy over that period.

Her most significant contribution has been leading the execution of the global Phase 3 PARAOA012 trial, which completed recruitment with 538 participants across the United States, Australia, Hong Kong and Moldova. Rather than departing, she continues with the company as Senior Scientific Advisor, where she will apply her extensive knowledge of iPPS to support Dr Furtner and the clinical team through the next stage.

Phase 3 enrolment completion came with 538 participants across 65 clinical sites in four countries, surpassing the original 466-participant target and locking in an Interim Analysis for September 2026 with top-line results expected in Q1 2027.

Dr Donna Skerrett

“…Completing recruitment into PARAOA012 has been one of the proudest achievements of my career. It reflects the extraordinary commitment of our clinical team, investigators, partners and, above all, the participants and their families.”

“I remain fully committed to Paradigm and excited by the potential of iPPS. I look forward to supporting Daniel through a seamless transition and continuing to contribute as Senior Scientific Advisor as we generate the clinical and scientific evidence that will guide the program’s next steps.”

What iPPS and the Phase 3 program mean for investors

iPPS (injectable pentosan polysulfate sodium), marketed under the brand name Zilosul®, is a subcutaneous treatment targeting inflammation and tissue regeneration. Paradigm is developing it primarily for osteoarthritis (Phase 3) and mucopolysaccharidosis (Phase 2).

Phase 3 is the final large-scale human trial stage in the drug development lifecycle before a company can seek regulatory approval. Completing this stage successfully is the key prerequisite for a formal regulatory submission to bodies such as the US Food and Drug Administration (FDA) or the Therapeutic Goods Administration (TGA).

Phase 3 Clinical Progress Tracker: iPPS (Zilosul®)

The Phase 3 journey — where Paradigm stands:

  1. Trial design and regulatory preparation (complete)
  2. Patient recruitment — 538 participants enrolled (complete)
  3. Clinical evidence generation (current phase)
  4. Regulatory submission preparation (next milestone)

The significance of this leadership transition lies in the profile Dr Furtner brings. A CMO with deep medical affairs and international clinical study experience is well suited to the shift from trial execution to assembling the evidence package required for regulatory submission.

Element Detail
Drug candidate iPPS (Zilosul®)
Trial PARA_OA_012 (Phase 3)
Indication Osteoarthritis
Participants enrolled 538
Sites US, Australia, Hong Kong, Moldova

Leadership continuity as the program enters its next stage

The structure Paradigm has put in place, with Dr Furtner leading medical strategy and Dr Skerrett continuing as Senior Scientific Advisor, represents a deliberate approach to knowledge retention at a consequential point in the program. The company retains the institutional knowledge accumulated through years of trial design and execution while adding the regulatory and medical affairs expertise required for the next phase.

For investors, the picture is a late-stage biotech with a fully recruited Phase 3 trial and a purpose-built medical leadership team now focused on generating the clinical and scientific evidence that will guide the program toward regulatory submission. As noted in Paradigm’s FY26 Annual Report, this transition reflects the program’s progression rather than a change in strategic direction.

Pro forma cash runway of approximately $45 million following the upsized $14 million placement is expected to fund Paradigm’s operations through to the end of CY2026, covering the Phase 3 interim analysis without requiring additional dilutive equity under the current plan.

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Frequently Asked Questions

Who has Paradigm Biopharmaceuticals appointed as Chief Medical Officer?

Paradigm Biopharmaceuticals has appointed Dr Daniel Furtner as Chief Medical Officer, effective 16 September 2026. Dr Furtner brings over 20 years of pharmaceutical leadership experience, most recently as Senior Director of Medical Affairs (Asia Pacific) at CSL, with prior roles at AbbVie and Janssen across Europe, Asia, and Australia.

What is the PARA_OA_012 Phase 3 trial and where does it stand?

PARA_OA_012 is Paradigm's global Phase 3 clinical trial evaluating injectable pentosan polysulfate sodium (iPPS; Zilosul®) for osteoarthritis. Recruitment is complete with 538 participants enrolled across 65 sites in the US, Australia, Hong Kong, and Moldova, with an Interim Analysis scheduled for September 2026 and top-line results expected in Q1 2027.

What happens to Dr Donna Skerrett after the CMO transition at Paradigm?

Dr Donna Skerrett, who served as Paradigm's CMO since September 2019 and led the execution of the Phase 3 trial, transitions to the role of Senior Scientific Advisor. She remains with the company to support Dr Furtner and the clinical team through the evidence generation and regulatory submission preparation phases.

What is iPPS and what conditions is Paradigm developing it for?

iPPS, or injectable pentosan polysulfate sodium, is a subcutaneous treatment targeting inflammation and tissue regeneration, marketed under the brand name Zilosul®. Paradigm is developing it primarily for osteoarthritis in a Phase 3 trial and for mucopolysaccharidosis in a Phase 2 program.

How much cash does Paradigm Biopharmaceuticals have to fund its Phase 3 program?

Following an upsized $14 million placement, Paradigm holds a pro forma cash position of approximately $45 million, which is expected to fund operations through to the end of CY2026, covering the Phase 3 interim analysis without requiring additional dilutive equity under the current plan.

Josua Ferreira
By Josua Ferreira
Partnership Director
Josua Ferreira holds a Bachelor of Commerce in Marketing and Advertising and brings a background in publication, business development, and ASX market storytelling. He has worked with listed companies across the resource sector and broader market, combining sharp commercial instincts with a genuine commitment to keeping investors informed.
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