Pathalys Pharma Raises $150 Million in Secured Product Financing and Equity led by Abingworth; Forms Strategic Collaboration with Launch Therapeutics to Advance Upacicalcet through Pivotal Phase 3 Studies

Rhea-AI Summary

Pathalys Pharma has successfully raised $150 million through secured product financing and equity to support its phase 3 clinical trials for upacicalcet, designed for treating secondary hyperparathyroidism in dialysis patients. The financing was led by Abingworth with participation from Carlyle and OrbiMed. This funding will ensure Pathalys can proceed with pivotal studies and pre-commercialization activities. The partnership with Launch Therapeutics aims to leverage their clinical expertise, as they take lead roles in clinical trials while Pathalys manages manufacturing and regulatory interactions.

Positive

• Raised $150 million for phase 3 clinical trials and pre-commercialization of upacicalcet.
• Collaboration with Launch Therapeutics enhances clinical development capabilities.
• Upacicalcet shows promise based on successful phase 3 trials in Japan.

Negative

• None.

• Abingworth, a leading transatlantic life sciences investment firm and part of global investment firm Carlyle (NASDAQ: CG), led financings and was joined by Carlyle, OrbiMed, and Pathalys' founding investors Catalys Pacific and DaVita Venture Group
• Transaction is expected to fully fund upacicalcet through pivotal phase 3 studies and pre-commercialization activities
• Collaboration leverages clinical development experience of Launch Tx and Pathalys' extensive dialysis expertise to advance the upacicalcet development program

RESEARCH TRIANGLE PARK, N.C. and BOSTON, Jan. 18, 2023 /PRNewswire/ -- Pathalys Pharma, Inc., a private, late-stage biopharma company co-founded by Catalys Pacific and DaVita Venture Group, and Launch Therapeutics (Launch Tx), a clinical development company, today announced a collaboration to advance phase 3 clinical trials for upacicalcet (designated PLS240 for clinical trials) for the treatment of secondary hyperparathyroidism (SHPT) in patients on hemodialysis. Launch Tx is backed by funds managed by global investment firm Carlyle (NASDAQ: CG) and its life sciences franchise Abingworth.

Pathalys Pharma Raises $150 Million in Secured Product Financing and Equity 

Pathalys also announced it has raised $150 million through a combination of secured product financing and equity to support the two phase 3 clinical trials, registration efforts and pre-commercialization activities for upacicalcet. Abingworth led both financings and was joined by Carlyle and OrbiMed, along with Pathalys' founding investors Catalys Pacific and DaVita Venture Group. Pathalys retains worldwide commercial rights to upacicalcet, outside Japan and Asia, and has the option to prepay its obligations in full at any time.

"Pathalys is very excited to collaborate with Launch Tx and to have the backing of such an esteemed group of healthcare investors. Through this collaboration and transaction, Pathalys expects to be fully funded through the completion of its planned phase 3 trials, and pre-commercialization efforts for upacicalcet." said Neal Fowler, Chief Executive Officer at Pathalys. "We look forward to working closely with Launch Tx to advance upacicalcet toward registration in the U.S. with the goal of making this important product candidate available for dialysis patients with SHPT." 

The co-development agreement creates a collaboration that combines the exceptional clinical development resources available through Launch Tx and the extensive dialysis expertise of Pathalys to advance the upacicalcet clinical development program. Launch Tx will have the lead role in the operational execution and management of the planned clinical trials and Pathalys will retain primary responsibility for manufacturing, FDA regulatory interactions and commercialization. 

Anshul Thakral, CEO of Launch Tx, commented, "We are thrilled to collaborate with Pathalys to advance upacicalcet. Launch Tx will bring deep clinical and operational resources to this phase 3 program to accelerate the path to regulatory approval. We offer a unique approach that helps both pharma and biotech companies develop their late-stage therapies and plan to demonstrate that approach through our collaboration with Pathalys."

Earlier this year, Pathalys disclosed its plans to initiate two phase 3 clinical trials to evaluate upacicalcet as a treatment alternative to currently available calcimimetics. Upacicalcet is a novel calcimimetic that performed exceptionally well in phase 3 studies in Japan where it was approved last year for the treatment of SHPT in patients on dialysis. An intravenous calcimimetic like upacicalcet may allow patients on dialysis better control of serum parathyroid hormone levels in SHPT in a convenient and compliant way, without increasing their calcium-phosphorus production while, more importantly, lowering their risk for vascular calcifications.

About Upacicalcet

Upacicalcet is an intravenously administered investigational small molecule calcimimetic that may control intact parathyroid hormone (iPTH) levels in patients with secondary hyperparathyroidism (SHPT) receiving hemodialysis. Upacicalcet was granted Marketing Authorization in Japan in 2021, under the brand name UPASITA®, based on a phase 3, 24-week double-blind, placebo-controlled dose-titration study and a second phase 3, 52-week open-label, dose-titration study. In these studies, upacicalcet was shown to significantly reduce iPTH and maintain long-term iPTH suppression, as well as demonstrate the potential for fewer adverse events (AEs) than currently available therapies.

About Pathalys Pharma

Pathalys Pharma, Inc. is a private, late-stage clinical biopharmaceutical company committed to the development of multiple advanced therapeutics that address unmet needs in the management of end-stage kidney disease (ESKD). Pathalys' initial asset is upacicalcet, a novel calcimimetic with the potential to improve the treatment of SHPT in hemodialysis patients. Beyond upacicalcet, Pathalys continues to identify other high priority needs and potential solutions for patients with ESKD. Pathalys was co-founded by Catalys Pacific and DaVita Venture Group and is headquartered in Research Triangle Park, North Carolina.

For more information about Pathalys, please visit www.pathalys.com.

About Launch Therapeutics

Launch Therapeutics (Launch Tx) is a clinical development company with a mission to disrupt the late-stage development paradigm, accelerate timelines to regulatory success, and bring new medicines to patients faster. Launch Tx offers pharmaceutical and biotech companies a variety of innovative models that combine access to capital with deep drug development, medical, clinical operations, regulatory, and commercialization expertise. These models include significant risk financing, clinical co-development, and full in-licensing, all of which offer partners an aligned and efficient approach to realizing the potential of late-stage clinical programs across any therapeutic area. Founded in 2022, Launch Tx is backed by leading investors, Carlyle and its life sciences franchise, Abingworth, and is led by a committed, experienced team with an enthusiastic passion to fulfil its mission.

For more information, visit launchtx.com and follow us on LinkedIn.

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SOURCE Pathalys Pharma

FAQ

What is upacicalcet's purpose in phase 3 clinical trials?

Upacicalcet is being tested as a treatment for secondary hyperparathyroidism in patients undergoing hemodialysis.

Who led the financing for Pathalys Pharma's clinical trials?

The financing was led by Abingworth, with participation from Carlyle and OrbiMed.

What will the raised funds be used for?

The funds will support phase 3 clinical trials, registration efforts, and pre-commercialization activities for upacicalcet.

What are the expected outcomes of the collaboration with Launch Therapeutics?

The collaboration aims to leverage Launch Therapeutics' clinical development experience to accelerate the phase 3 trials of upacicalcet.

When was upacicalcet approved in Japan?

Upacicalcet received marketing authorization in Japan in 2021.