Skip to content

What does Cidara Therapeutics do? A Legacy in Biotech Explained

4 min read

As of August 2024, Cidara Therapeutics underwent a significant corporate restructuring, ultimately leading to its merger and rebranding as COSCIENS Biopharma Inc.. To truly understand what Cidara Therapeutics does, one must look at its history in developing innovative immunotherapies and anti-infectives.

Quick Summary

Cidara Therapeutics, which ceased independent operations and became part of COSCIENS Biopharma Inc. in 2024, utilized its Cloudbreak® platform to develop targeted immunotherapies for serious conditions like invasive fungal infections, influenza, and cancer.

Key Points

  • Cloudbreak Platform: Cidara's core technology was the Cloudbreak® platform, used to create novel drug-Fc conjugates (DFCs) targeting serious diseases.

  • REZZAYO® (rezafungin): A key product was the once-weekly antifungal rezafungin, approved for invasive candidiasis and licensed to commercial partners.

  • CD388 Influenza Antiviral: Cidara developed CD388, a long-acting antiviral candidate for universal influenza prevention, which showed promising clinical results.

  • Oncology Focus: The company expanded its pipeline into immuno-oncology with candidates like CBO421, targeting solid tumors.

  • Corporate Restructuring: In 2024, Cidara Therapeutics effectively ceased to exist as an independent entity following a merger involving Aeterna Zentaris.

  • Rebranded as COSCIENS: The legacy company and its assets were incorporated into COSCIENS Biopharma Inc. in August 2024, following a merger between Aeterna Zentaris and Ceapro Inc.

In This Article

A Retrospective on Cidara Therapeutics

Cidara Therapeutics, before its merger and subsequent name change, was a San Diego-based biotechnology company dedicated to the development of novel anti-infectives and immunotherapies for patients battling serious diseases. The company’s core innovation centered on its proprietary Cloudbreak® platform, which was used to create a unique class of therapeutics known as Drug-Fc Conjugates (DFCs). The company's journey was marked by significant clinical progress in multiple therapeutic areas, from successful antifungal treatments to promising influenza preventatives, before its strategic transformation.

The Cloudbreak® Platform: A Multi-Modal Approach

The Cloudbreak® platform was the technological cornerstone of Cidara's operations. This innovative system was designed to develop Drug-Fc Conjugates (DFCs), which are complex molecules that combine a targeted small molecule or peptide with a human antibody fragment (Fc). This "single molecule cocktail" approach offered a dual mechanism of action:

How Drug-Fc Conjugates (DFCs) Work

  • Targeted Inhibition: The small molecule or peptide component of the DFC specifically targets and inhibits disease pathways, such as a viral enzyme or a protein on a tumor cell.
  • Immune System Engagement: The Fc fragment, derived from a human antibody, is designed to engage the patient's immune system, directing immune cells to the site of the disease to help clear the pathogen or tumor. This combination was intended to maximize efficacy while reducing the need for combination therapies.

Leading the Way in Antifungal and Antiviral Treatments

Before focusing entirely on its Cloudbreak pipeline, Cidara successfully developed and licensed a groundbreaking antifungal agent.

Rezafungin: The Antifungal Success Story

One of Cidara's most significant achievements was the development of rezafungin (marketed as REZZAYO™), a once-weekly echinocandin for the treatment of invasive candidiasis and candidemia. This product represented a notable advance over previous standard-of-care treatments by offering a weekly dosing regimen, which simplified administration. Cidara completed Phase 3 clinical trials for rezafungin, and it was ultimately approved by the FDA and European Commission. The company licensed commercial rights for rezafungin to partners, such as Melinta Therapeutics in the U.S., allowing Cidara to focus on its DFC pipeline.

CD388: A Novel Approach to Influenza Prevention

In the realm of antivirals, Cidara's lead DFC candidate was CD388, a long-acting therapeutic designed for the universal prevention of seasonal and pandemic influenza. Unlike traditional vaccines, CD388 is not reliant on an immune response, making it potentially effective for immunocompromised individuals.

Key advantages of CD388 over traditional vaccines:

  • Universal Protection: Designed to provide activity against all influenza A and B strains.
  • Long-Lasting Effect: Intended to provide season-long protection with a single dose.
  • Immune Status Independent: Efficacy was not reliant on the patient's existing immune response, a significant benefit for high-risk populations.

Clinical trials, including the Phase 2b NAVIGATE trial, demonstrated positive top-line results for CD388, reinforcing the potential of the Cloudbreak platform. You can find more information about the preclinical development of CD388 on the Nature website.

Advancing into Oncology

Beyond infectious diseases, Cidara leveraged its Cloudbreak platform to explore novel immuno-oncology treatments. The company developed DFCs that acted as "single molecule cocktails" to target cancer and activate the immune system simultaneously.

CBO421: Targeting CD73 in Solid Tumors

One of Cidara's key oncology candidates was CBO421, which targeted the CD73 enzyme. This enzyme is known to suppress the anti-tumor immune response within the tumor microenvironment. By targeting CD73, CBO421 was designed to create a more favorable environment for the immune system to fight cancer. Cidara received investigational new drug (IND) clearance for CBO421 in July 2024, marking a significant step in its oncology program.

The Corporate Transformation: From Cidara to COSCIENS

The history of Cidara Therapeutics took a dramatic turn in 2024 through a series of corporate events that led to its effective dissolution and re-emergence under a new name.

In early 2024, Aeterna Zentaris completed a merger with Ceapro Inc.. Aeterna had previously acquired Cidara, and this subsequent merger created a new entity. This new biopharmaceutical company, combining the assets of Aeterna Zentaris, Ceapro, and the legacy of Cidara, was renamed COSCIENS Biopharma Inc., effective August 6, 2024. This move created a diversified biopharma company with a broader portfolio, including the Cloudbreak technology platform.

Cidara's Legacy: A Comparison of Therapeutic Approaches

Cidara's DFC technology offered a differentiated approach compared to traditional methods. The following table highlights some key distinctions:

Feature Cidara's DFCs (e.g., CD388) Traditional Vaccines Standard Antivirals (e.g., oseltamivir)
Mechanism Dual-action: Viral inhibition + immune engagement Single-action: Elicits immune response Single-action: Viral inhibition
Protection Universal, against multiple strains Strain-specific, requires annual update Often strain-specific, resistance can develop
Timing Immediate protection, not relying on immune response Delayed, relies on body building immunity Takes effect after symptoms appear
Population Effective in both healthy and immunocompromised patients May be less effective in immunocompromised patients Can be used broadly, but resistance is a concern
Administration Single, long-acting dose Annual vaccination required Requires multiple daily doses during illness

Conclusion

What did Cidara Therapeutics do? It successfully developed and brought to market a novel antifungal and pioneered a new class of targeted immunotherapies through its Cloudbreak® platform. While the Cidara name no longer exists in the corporate landscape, its scientific legacy and innovative platform continue under the new banner of COSCIENS Biopharma Inc. The story of Cidara highlights the dynamic and evolving nature of the biotechnology industry, where cutting-edge technology platforms can change hands and shape the future of medical treatments under new corporate structures.

Frequently Asked Questions

Cidara Therapeutics was a biotechnology company that developed targeted immunotherapies and anti-infectives. The company's main technology was its Cloudbreak® platform, which created Drug-Fc Conjugates (DFCs).

In 2024, Cidara Therapeutics was effectively integrated into a larger corporate structure. Through a series of mergers involving Aeterna Zentaris and Ceapro Inc., the combined entity was rebranded as COSCIENS Biopharma Inc., effective August 6, 2024.

Cidara focused on serious diseases, including invasive fungal infections, seasonal and pandemic influenza, and various cancers using its advanced DFC platform.

The Cloudbreak® platform was Cidara's proprietary technology for developing Drug-Fc Conjugates (DFCs). These compounds combine a targeted molecule with an antibody fragment to both inhibit disease targets and engage the patient's immune system.

Yes, Cidara developed and received FDA approval for REZZAYO™ (rezafungin for injection), a once-weekly antifungal treatment. The commercial rights for this drug were licensed to partners like Melinta Therapeutics.

COSCIENS Biopharma Inc. is the new name for the company that resulted from the merger of Aeterna Zentaris and Ceapro Inc. in 2024, incorporating the assets and legacy of the former Cidara Therapeutics.

Rezafungin was significant because it was a long-acting, once-weekly echinocandin, offering a more convenient dosing schedule than older antifungals for treating invasive candidiasis and candidemia.

Yes. Cidara was developing CD388, a long-acting, non-vaccine antiviral for universal influenza prevention that showed promise in clinical trials for protecting against various flu strains.

References

  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7
  8. 8
  9. 9
  10. 10

Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.