Active, not recruitingPhase I/IIEN originalLung cancerHER2 positiveMetastatic / advanced

A Study of BL-M07D1 in Patients With HER2-mutated, Locally Advanced or Metastatic Non-small-cell Lung Cancer

⚠️

This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

This trial is no longer recruiting — here are similar active trials

Matched by cancer type/biomarker, currently recruiting.

RecruitingUnknown phase🇵🇱 PolandFemale onlyOvarian cancerCervical cancerOther cancersMetastatic / advanced

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.

RecruitingNot applicable🇵🇱 PolandLung cancer

In this phase III study, the primary objective is to test with a one-sided significance of 5% whether for the treatment of small cell lung cancer (SCLC) patients, brain MRI surveillance alone is non-inferior in terms of overall survival compared to prophylactic cranial irradiation (PCI) combined with brain MRI surveillance in the entire study population.

RecruitingPhase III🇵🇱 PolandMale onlyProstate cancerMetastatic / advanced

The primary objective of this study is to measure efficacy of saruparib + physician's choice of ARPI compared with placebo + ARPI in men with metastatic hormone-sensitive prostate cancer (mHSPC) who have previously received docetaxel chemotherapy or a prostate-specific membrane antigen (PSMA)-directed lutetium-177 radioligand therapy with no evidence of disease progression and PSA ≥ 0.2 ng/mL.

About the trial

This phase Ib/II study is designed to evaluate the safety, tolerability, pharmacokinetics, and efficacy of injectable BL-M07D1 in patients with HER2-mutated, locally advanced or metastatic non-small cell lung cancer.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • •Wiek od 18 do 75 lat
  • •Potwierdzony zaawansowany rak płuca non-small cell, którego nie można operować
  • •Potwierdzona mutacja HER2 w komórkach raka
  • •Wcześniej leczony chemioterapią lub immunoterapią, bez efektu lub ze skutkami ubocznymi
  • •Przytomność i możliwość samodzielnej opieki (wynik ECOG 0-1)
  • •Funkcjonowanie serca w normie (frakcja wyrzutowa ≥50%)
  • •Przynajmniej jeden zmierzalny guz według dostępnych badań
  • •Chęć udziału i podpisanie zgody na badanie

✗ Disqualifies

  • •Brak informacji o kryteriach wykluczających w pełnym tekście źródła

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Maximum age
75 Years
Last updated (source)
September 21, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (1)

Sun Yat-sen University Cancer Center

Guangzhou, China

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/24/2026.

You can help another person

We fund the Radar, this site, and the development of our Grosz dla Życia fundraising platform from donations and our own resources. Every contribution, even a small one, really helps.