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Chugai Pharmaceutical
Traitements, essais et publications liés.
Traitements4programmes
Essais2liés
Publications3liées
SourceDBlocale
Traitements
4| Molécule | Indication / population | Phase | Objectif | Pays | Résultat |
|---|---|---|---|---|---|
| AQUA07This is a first-in-human, Phase I, open-label, multicenter, multinational study, designed to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and anti-tumor activity of AQUA07 when administered as single agent and in combination with lorlatinib in patients with ALK positive non-small cell lung cancer. | Cancer | Phase 1 | À vérifier | United States, Japan | À vérifier |
| LorlatinibThis study will test the safety of the combination of ramucirumab and lorlatinib. The researchers will test one or two different doses of lorlatinib in combination with ramucirumab to find the drug combination dose that causes few or mild side effects in participants. Once the researchers find this dose, they can test it in future participants to see if it is effective in treating their metastatic ALK-rearranged NSCLC. The researchers are also looking to see whether there are specific genes or DNA sequences associated with a response to treatment with lorlatinib and ramucirumab. | Cancer | Phase 1 | À vérifier | United States, Japan | À vérifier |
| LorlatinibThis study will test the safety of the combination of ramucirumab and lorlatinib. The researchers will test one or two different doses of lorlatinib in combination with ramucirumab to find the drug combination dose that causes few or mild side effects in participants. Once the researchers find this dose, they can test it in future participants to see if it is effective in treating their metastatic ALK-rearranged NSCLC. The researchers are also looking to see whether there are specific genes or DNA sequences associated with a response to treatment with lorlatinib and ramucirumab. | Cancer | Phase 1 | À vérifier | United States | À vérifier |
| AQUA07This is a first-in-human, Phase I, open-label, multicenter, multinational study, designed to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and anti-tumor activity of AQUA07 when administered as single agent and in combination with lorlatinib in patients with ALK positive non-small cell lung cancer. | Cancer | Phase 1 | À vérifier | United States, Japan | À vérifier |
Essais cliniques
2| Molécule | Indication / population | Phase | NCT | Titre | Statut |
|---|---|---|---|---|---|
| AQUA07 | Cancer | Phase 1 | NCT07617337 | AQUA07 in Patients With ALK-Positive Non-Small Cell Lung Cancer | RECRUITING |
| Lorlatinib | Cancer | Phase 1 | NCT06007937 | A Study of Lorlatinib in Combination With Ramucirumab in People With Lung Cancer | ACTIVE_NOT_RECRUITING |
Publications
3| Molécule | Indication / population | Titre | Journal | Date |
|---|---|---|---|---|
| Lorlatinib | Cost-effectiveness analysis of lorlatinib as first-line treatment for anaplastic lymphoma kinase (ALK)-positive non-small cell lung cancer in Italy. | Journal of medical economics | ||
| Lorlatinib | Cost of managing brain metastases in patients with ALK+ advanced NSCLC with first-line tyrosine kinase inhibitors in the UK. | Lung cancer management | ||
| Lorlatinib | Clinical characteristics of ALK-positive NSCLC patients treated with sequential ALK-TKI therapies in a single-centre. | Lung cancer management |