VISION: An international, prospective, open-label, multicenter, randomized phase 3 study of 177 Lu-PSMA-617 in the treatment of patients with progressive PSMA-positive metastatic castration

VISION investigators aim to complete data collection for the primary outcome measures in May 2020. 11 Positive results from this trial could facilitate the FDA approval of 177 Lu-PSMA-617 for use in patients with mCRPC who have no or few treatment options.

If completed, the Endocyte acquisition would expand the Novartis RLT platform with both a potential near-term product launch and early-stage clinical development programs. Kabasakal et al. Pre-therapeutic dosimetry of normal organs and tissues of (177)Lu-PSMA-617 prostate-specific membrane antigen (PSMA) inhibitor in patients with castration-resistant prostate cancer. Eur J Nucl Med Mol Imaging. 2015 Dec;42(13):1976-83 Radioligand Therapy using 177Lu-PSMA-617 Dosimetry 23 Mar 2021 Lu-PSMA-617, a targeted radioligand therapy, demonstrated The company also announced that results from the VISION trial will be 23 Mar 2021 In the Phase III VISION trial, researchers examined the efficacy and safety of 177 Lu-PSMA-617, an investigational PSMA-targeted radioligand 25 Jun 2020 We eagerly await results of the upcoming phase III VISION trial, which will tell us Lu-177–PSMA-617 is the furthest along in development of 23 Mar 2021 The addition of the targeted radioligand therapy 177Lu-PSMA-617 to best cancer, meeting both primary end points of the phase 3 VISION trial.

2021-03-23 Swiss drug major Novartis AG announced Tuesday positive result from its phase III VISION study evaluating the efficacy and safety of radioligand therapy 177Lu-PSMA-617 in patients with advanced prostate cancer.The trial met both primary endpoints of overall survival and radiographic progression-free survival. The company noted that the safety profile was consistent with data reported in 2017-02-06 One of these is a phase 3 trial called VISION (Study of 177 Lu-PSMA-617 in Metastatic Castrate-Resistant Prostate Cancer; NCT03511664). For this trial, researchers are randomly assigning 750 patients with progressive PSMA-positive metastatic castration-resistant prostate cancer to 177 Lu-PSMA-617 or best standard of care. We saw recently (see this link) that of chemo and hormonal medicines for metastatic castration-resistant prostate cancer (mCRPC), Jevtana (cabazitaxel) is the preferred third treatment after Taxotere (docetaxel) and Zytiga (abiraterone) or Xtandi (enzalutamide).But when should radiopharmaceuticals, either approved ones like Xofigo (Ra-223), or prospective ones like Lu-177-PSMA-617, be used in 2018-10-18 2021-03-23 If [the VISION study] is positive, then Lu-PSMA-617 could have a considerable impact on care for that space. What other agents are emerging in prostate cancer? There are a variety of agents that 2017-10-17 With the recent favorable data on PSMA radioligands confirming the value of PSMA targeting and radionuclide therapy, our current goal is to further optimize this therapeutic approach with a series of early phase trials running in parallel.

DOI: 10.1007/s00259-020-04703-3 Corpus ID: 211127815. Radioligand therapy using [177Lu]Lu-PSMA-617 in mCRPC: a pre-VISION single-center analysis @article{Seifert2020RadioligandTU, title={Radioligand therapy using [177Lu]Lu-PSMA-617 in mCRPC: a pre-VISION single-center analysis}, author={R.

2021-04-11

Kabasakal L, AbuQbeitah M, Aygün A, et al. Pre-therapeutic dosimetry of normal organs and tissues of 177Lu-PSMA-617 prostate-specific membrane antigen NCI supports clinical trials that test new and more effective ways to treat cancer. Find clinical trials studying lutetium lu 177-psma-617. 23 Jul 2020 If the results of the ongoing, international phase III VISION trial on 177Lu-PSMA- 617 plus best standard of care versus only chemotherapy best First prospective trial with 177Lu-PSMA-617 in mCRPC.

2018-10-25 · The trial (also known as the VISION study) is nominally being sponsored by Endocyte (the developer of 177 Lu-PSMA-617), but Endocyte recently agreed to being acquired by Novartis, and so — to all practical intents and purposes — Novartis is now the effective sponsor of this trial (unless the deal falls through).

– Tomma lokaler. 4 413. 2 500. 177Lu-DOTATATE peptide receptor radionuclide therapy: dose response in small intestinal Ingår i Journal of Mathematical Imaging and Vision, s. Comparison of 68Ga-PSMA-11 PET/CT with 11C-acetate PET/CT in 609-617, 2019. vilken den placerade sitt dotterbolag CIBA VISION och Novartis Ophthalmics, Lu -PSMA-617 riktad mot metastaserad kastreringsresistent prostatacancer.

NeoRay: [177Lu]-NeoB in Patients 8. Kabasakal L, AbuQbeitah M, Aygün A, et al. Pre-therapeutic dosimetry of normal organs and tissues of 177Lu-PSMA-617 prostate-specific membrane antigen NCI supports clinical trials that test new and more effective ways to treat cancer. Find clinical trials studying lutetium lu 177-psma-617. 23 Jul 2020 If the results of the ongoing, international phase III VISION trial on 177Lu-PSMA- 617 plus best standard of care versus only chemotherapy best First prospective trial with 177Lu-PSMA-617 in mCRPC.
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1 Basel, March, 23, 2021 — Novartis today reported the first interpretable results of the Phase III VISION study evaluating the efficacy and safety of 177 Lu-PSMA-617, a targeted radioligand therapy The addition of the targeted radioligand therapy 177Lu-PSMA-617 to best standard of care was found to significantly improve overall survival (OS) and radiographic progression-free survival (rPFS) We have just been appraised of a randomized, double-blind, multi-center, Phase III clinical trial of the targeted, radiolabeled agent 177 Lu-PSMA-617 (a form of “radioligand” therapy) in the treatment of metastatic, castration-resistant prostate cancer (mCRPC). Details about this trial can be found on the ClinicalTrials.gov web site. (RTTNews) - Swiss drug major Novartis AG (NVS) announced Tuesday positive result from its phase III VISION study evaluating the efficacy and safety of radioligand therapy 177Lu-PSMA-617 in Jason M. Broderick Adding the targeted radioligand therapy 177 Lu-PSMA-617 (LuPSMA) to best standard of care (BSC) improved overall survival (OS) in patients with progressive PSMA-positive metastatic castration-resistant prostate cancer (mCRPC), according to findings from the phase 3 VISION trial. 1 Basel, March, 23, 2021 — Novartis today reported the first interpretable results of the Phase III VISION study evaluating the efficacy and safety of 177 Lu-PSMA-617, a targeted radioligand therapy March, 23, 2021: “Novartis reported the first interpretable results of the Phase III VISION study evaluating the efficacy and safety of 177 Lu-PSMA-617, a targeted radioligand therapy in patients with progressive PSMA-positive metastatic castration-resistant prostate cancer (mCRPC) compared to best standard of care alone. In the international, prospective, open-label, multicenter VISION trial, investigators set out to compare OS in patients with progressive PSMA-positive mCRPC who receive 177 Lu-PSMA-617 plus best BACKGROUND: Radioligand therapy with [177Lu]Lu-PSMA-617 is efficacious for the treatment of patients with metastasized castration-resistant prostate cancer (mCRPC).

For this trial, researchers are randomly assigning 750 patients with progressive PSMA-positive metastatic castration-resistant prostate cancer to 177 Lu-PSMA-617 or best standard of care. We saw recently (see this link) that of chemo and hormonal medicines for metastatic castration-resistant prostate cancer (mCRPC), Jevtana (cabazitaxel) is the preferred third treatment after Taxotere (docetaxel) and Zytiga (abiraterone) or Xtandi (enzalutamide).But when should radiopharmaceuticals, either approved ones like Xofigo (Ra-223), or prospective ones like Lu-177-PSMA-617, be used in 2018-10-18 2021-03-23 If [the VISION study] is positive, then Lu-PSMA-617 could have a considerable impact on care for that space.
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15 Jul 2020 177Lu-PSMA-617 is in clinical development for patients with metastatic castration - resistant indication. The ongoing trial phase III clinical trial (VISION, NCT03511664) has an estimated treatment with 177-Lu-PSMA-

This evidence supports the need for randomised controlled trials to further assess efficacy compared with current standards of care. 2 dagar sedan · 177Lu-PSMA-617 is a radioligand therapy (RLT) being developed by Novartis (acquired from Endocyte) that utilizes a high affinity targeting ligand to direct potent radiotherapy to prostate cancer cells. The specific targeting of this therapy comes from the “ligand” portion of the RLT, which is a 177 Lu-PSMA-617 Radioligand Therapy in Metastatic Castration-Resistant Prostate Cancer Patients with a Single Functioning Kidney J Nucl Med . 2019 Nov;60(11):1579-1586. doi: 10.2967/jnumed.118.223149. Phase III VISION study with 177Lu-PSMA-617 met both primary endpoints, significantly improving overall survival (OS) and radiographic progression-free survival (rPFS) in patients with PSMA-positive metastatic castration-resistant prostate cancer1 VISION trial findings to be presented at upcoming medical meeting, with regulatory submissions in the US and EU anticipated in 2021 Novartis is 2020-08-26 · According to the studied procedures in the VISION study, mCRPC patients will be eligible for treatment once every 6 weeks with a maximum of 6 cycles of 7.4 GBq [177 Lu]Lu-PSMA-617. TheraP, another clinical phase 2 trial (NCT03392428) initiated by Endocyte/Novartis, aims to determine the activity and safety of [ 177 Lu]Lu-PSMA-617 RLT as a second line treatment and will be performed in Australia.