News | SPECT Imaging | February 05, 2025

Company receives positive feedback on Phase III trial design.


Feb. 5, 2025 — Serac Healthcare Ltd., a clinical radiopharmaceutical company developing an innovative molecular imaging agent, said it has received positive feedback from its End of Phase II Meeting with the US Food and Drug Administration (FDA) for the development of 99mTc-maraciclatide as a diagnostic agent for use with single-photon emission computed tomography (SPECT-CT) for the visualization and diagnosis of superficial peritoneal endometriosis (SPE) in women aged 16 years of age and older.

Initial Phase II findings indicate that 99mTc-maraciclatide has potential as a non-invasive test for the detection of SPE. SPE is not well visualized with current non-invasive imaging tools (ultrasound and MRI) and definitive diagnosis requires laparoscopy. The planned Phase III study will compare the findings from women undergoing laparoscopic surgery for endometriosis with imaging using 99mTc-maraciclatide and SPECT-CT prior to surgery.

The FDA feedback on the Phase III study design follows their review of the Phase II results and builds on the grant of Fast Track Designation to 99mTc maraciclatide in July 2024 as a diagnostic agent for use with SPECT-CT for the visualization and diagnosis of SPE in women of 16 years and older.

David Hail, Chief Executive of Serac Healthcare, commented, "We are delighted with the outcome of our End of Phase II Meeting with the FDA which provides us with a clear development path for maraciclatide. We are looking forward to finalizing the Phase III protocol with the FDA.”

“Chronic pain, fertility issues and depression are just some of the consequences that one in ten women with endometriosis are living with every day. A non-invasive test, particularly for early-stage disease which cannot easily be visualized by other imaging methods, and which accounts for eighty per cent of diagnoses by laparoscopic surgery, is desperately needed by the 190 million women worldwide suffering from this debilitating condition.”

The company is now finalizing the protocol and will be working with the FDA to prepare for the start of the Phase III program.

For more imformation, please visit www.serachealthcare.com.


Related Content

News | Radiology Imaging

April 7, 2026 — Onvida Health and Siemens Healthineers have entered a 10-year Value Partnership¹ designed to bring the ...

Time April 09, 2026
arrow
News | Computed Tomography (CT)

April 2, 2026 — GE HealthCare has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for True ...

Time April 03, 2026
arrow
News | Ultrasound Imaging

March 30, 2026 — Butterfly Network, Inc. has received clearance from the U.S. Food and Drug Administration (FDA) for a ...

Time April 01, 2026
arrow
News | Radiology Business

March 31, 2026 — Radon Medical Imaging, a medical imaging equipment maintenance and repair services company, has has ...

Time March 31, 2026
arrow
News | Radiology Imaging

March 26, 2026 — GE HealthCare has announced a renewed research collaboration with Stanford Medicine Department of ...

Time March 30, 2026
arrow
News | Cardiac Imaging

March 28, 2026 — When Ashley Perlow felt a sharp pain shoot across her chest and into both wrists, she didn't think it ...

Time March 30, 2026
arrow
News | FDA

March 24, 2026 — MARS Bioimaging, a New Zealand–headquartered medical device company, has received U.S. Food and Drug ...

Time March 25, 2026
arrow
News | Radiology Imaging

March 23, 2026 — Samsung Medison hsa announced that its U.S. medical imaging businesses, previously operating as ...

Time March 23, 2026
arrow
News | Breast Imaging

March 10, 2026 — QT Imaging Holdings has received U.S. Food and Drug Administration (FDA) 510(k) clearance for an ...

Time March 13, 2026
arrow
News | Enterprise Imaging

Mar. 9, 2026 — GE HealthCare recently announced that View, the viewer within the Genesis Radiology Workspace, has ...

Time March 12, 2026
arrow
Subscribe Now