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BioWorld - Tuesday, February 3, 2026
Home » PET imaging agents

Articles Tagged with ''PET imaging agents''

Diagnostics

US researchers divulge new PET and SPECT imaging agents

Dec. 1, 2025
Cornell University and The General Hospital Corp. (Massachusetts General Hospital) have synthesized conjugates comprising a targeting moiety covalently linked to a radiolabeled metal chelator through a linker acting as positron emission tomography (PET) or single-photon emission computerized tomography (SPECT) imaging agents reported to be useful for diagnosis and treatment of cancer.
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FDA approved icons and medical professional

Have kit, will travel further: Telix PET-imaging agent approved by FDA

March 25, 2025
By Lee Landenberger
The U.S. FDA’s approval of Telix Pharmaceuticals Ltd.’s kit for preparing prostate-specific membrane antigen-PET imaging for prostate cancer widens the opportunities for patients who live far away from large hospitals. The FDA’s nod for the imaging agent, TLX007-CDx, now branded as Gozellix, has a long shelf life and needs less equipment and preparation compared to some other agents.
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FDA approved icons and medical professional

Have kit, will travel further: Telix PET-imaging agent approved by FDA

March 21, 2025
By Lee Landenberger
The U.S. FDA’s approval of Telix Pharmaceuticals Ltd.’s kit for preparing prostate-specific membrane antigen-PET imaging for prostate cancer widens the opportunities for patients who live far away from large hospitals. The FDA’s nod for the imaging agent, TLX007-CDx, now branded as Gozellix, has a long shelf life and needs less equipment and preparation compared to some other agents.
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Illustration of tumor on kidney

FDA accepts Telix BLA for kidney cancer imaging agent

March 4, 2025
By Tamra Sami
After a second round, the U.S. FDA has accepted for review radiopharmaceutical company Telix Pharmaceuticals Ltd.’s BLA for its kidney cancer PET imaging agent, TLX250-CDx (Zircaix, 89Zr-DFO-girentuximab), granting it a priority review with a PDUFA date of Aug. 27, 2025.
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Illustration of tumor on kidney

FDA accepts Telix BLA for kidney cancer imaging agent

Feb. 27, 2025
By Tamra Sami
After a second round, the U.S. FDA has accepted for review radiopharmaceutical company Telix Pharmaceuticals Ltd.’s BLA for its kidney cancer PET imaging agent, TLX250-CDx (Zircaix, 89Zr-DFO-girentuximab), granting it a priority review with a PDUFA date of Aug. 27, 2025.
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Illustration of tumor on kidney

FDA accepts Telix BLA for kidney cancer imaging agent

Feb. 26, 2025
By Tamra Sami
After a second round, the U.S. FDA has accepted for review radiopharmaceutical company Telix Pharmaceuticals Ltd.’s BLA for its kidney cancer PET imaging agent, TLX250-CDx (Zircaix, 89Zr-DFO-girentuximab), granting it a priority review with a PDUFA date of Aug. 27, 2025.
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3D structure model of α-synuclein
Diagnostics

Candidate tracer for α-synuclein imaging falls flat

Dec. 20, 2024
In a recently published study, researchers from the University of Pennsylvania and collaborators aimed to identify compounds with high affinity to α-synuclein aggregates and high selectivity toward pathological α-synuclein compared to other brain targets.
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Diagnostics

Researchers in the Netherlands describe new PET and SPECT imaging agents

Dec. 11, 2024
Researchers at Stichting AMC Foundation and Vrije Universiteit van Amsterdam have identified [18F]-labeled pyrazolidine-3,5-dione compounds targeting P2Y purinoceptor 12 (P2RY12; P2Y12) acting as PET and SPECT imaging agents. They are reported to be useful for the diagnosis of multiple sclerosis, Alzheimer’s disease and Parkinson’s disease.
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Diagnostics

Norroy Bioscience describes drug conjugates targeting FOLH1

Sep. 9, 2024
Norroy Bioscience Co. Ltd. has prepared drug conjugates comprising a radionuclide linked to a ligand targeting glutamate carboxypeptidase II (NAALADase; NAAG peptidase, FOLH1; PSMA) through a linker for use as positron-emission tomography (PET) imaging agents.
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Diagnostics

Abbvie scientists describe new PET imaging agents for progressive supranuclear palsy

March 28, 2024
Scientists from Abbvie Deutschland GmbH & Co. KG and Abbvie Inc. have identified radiolabeled compounds capable of imaging and targeting microtubule-associated protein Tau (PHF-tau; MAPT) aggregates acting as positron emission tomography (PET) imaging agents reported to be useful for the diagnosis of progressive supranuclear palsy.
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