REGYNERA(dia)TION is an international, multicenter, ambispective observational patient registry of adults with recurrent gynecologic malignancies after prior radiotherapy who are treated or planned for reirradiation and/or total ablative strategies as part of routine clinical care. The registry does not assign treatment. Radiotherapy technique, dose, systemic therapy, surgery, metastasis-directed therapy, imaging, and follow-up are selected by the treating multidisciplinary team according to local standards and patient-specific factors. The registry will collect harmonized retrospective and prospective data on disease characteristics, prior radiotherapy, recurrence pattern, reirradiation or ablative treatment exposure, response, progression, survival, severe treatment-related morbidity, fistula events, and patient-reported outcomes where available.
Rollover Study for Participants Who Have Been Treated With and Are Continuing to Benefit From Opnurasib as a Single Agent or in Combination With Other Study Treatments
This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.
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About the trial
The purpose of this study is to allow continued access to opnurasib (JDQ443) to participants who are benefitting from treatment with opnurasib as a single agent or in combination with other study treatments in pre-defined Novartis-sponsored opnurasib studies and to continue to assess safety in these participants.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Uczestnik jest obecnie leczony opnurasibem w ramach wcześniejszego badania firmy Novartis
- •Uczestnik otrzymał co najmniej 6 cykli leczenia opnurasibem w poprzednim badaniu
- •Leczenie przynosi pacjentowi wyraźną korzyść, według oceny lekarza prowadzącego
- •Pacjent wykazuje zmniejszenie tempa postępu choroby, poprawę objawów lub lepszą jakość życia
✗ Disqualifies
- •Pacjent został wcześniej na stałe wycofany z leczenia opnurasibem bez powodu przejścia do tego badania
- •Pacjent nie chce stosować się do wymogów antykoncepcji
- •Pacjent ma nierozwiązane działania niepożądane, które spowodowały wstrzymanie leczenia
- •U pacjenta zidentyfikowano mutacje, dla których dostępne są inne sprawdzone sposoby leczenia
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Maximum age
- 100 Years
- Last updated (source)
- October 15, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (21)
Novartis Investigative Site
Sint-Niklaas, Belgium
Novartis Investigative Site
Leuven, Belgium
Novartis Investigative Site
Montreal, Canada
Novartis Investigative Site
Sherbrooke, Canada
Novartis Investigative Site
Guangzhou, China
Novartis Investigative Site
Changsha, China
Novartis Investigative Site
Copenhagen, Denmark
Novartis Investigative Site
Bron, France
Novartis Investigative Site
Saint-Herblain, France
Novartis Investigative Site
Villejuif, France
Novartis Investigative Site
Milan, Italy
Novartis Investigative Site
Milan, Italy
Novartis Investigative Site
Roma, Italy
Novartis Investigative Site
Kashiwa, Japan
Novartis Investigative Site
Koto Ku, Japan
Novartis Investigative Site
Kuching, Malaysia
Novartis Investigative Site
Seoul, South Korea
Novartis Investigative Site
Pamplona, Spain
Novartis Investigative Site
Barcelona, Spain
Novartis Investigative Site
Madrid, Spain
Novartis Investigative Site
Valencia, Spain
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/14/2026.
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