INSTITUT CURIE
- Country
- 🇫🇷France
- Ownership
- Private
- Established
- 1909-01-01
- Employees
- 1K
- Market Cap
- -
- Website
- http://www.curie.fr
Clinical Trials
163
Trial Phases
6 Phases
Drug Approvals
0
Drug Approvals
No drug approvals found
This company may not have drug approvals in our database
Clinical Trials
Distribution across different clinical trial phases (137 trials with phase data)• Click on a phase to view related trials
Cutting Edge Imaging With PET-FAPI for Earlier Pancreatic Cancer Diagnosis
- Conditions
- Pancreatic Ductal Adenocarcinoma (PDAC)
- Interventions
- Drug: 68Ga-FAPI-46 for PET / CT scan and 177Lu-EB-FAPI for therapy
- First Posted Date
- 2024-10-26
- Last Posted Date
- 2025-06-25
- Lead Sponsor
- Institut Curie
- Target Recruit Count
- 35
- Registration Number
- NCT06659705
- Locations
- 🇫🇷
Institut Curie -site Saint-Cloud, Saint-cloud, France
Comparative Evaluation of Care Strategies on Dressing Change-induced Bleeding in Patients With Bleeding Malignant Wounds
- Conditions
- Malignant Wound
- First Posted Date
- 2024-09-03
- Last Posted Date
- 2025-03-28
- Lead Sponsor
- Institut Curie
- Target Recruit Count
- 108
- Registration Number
- NCT06581809
- Locations
- 🇫🇷
EHPAD Laurent Antoine, Agde, France
🇫🇷Hôpital Saint-Loup, Agde, France
🇫🇷Centre François Baclesse, Caen, France
Efficacy of Personalized Tumorogram-based Therapy in Cancer Established From Patient-derived Organoid
- Conditions
- Metastatic Breast Cancer
- First Posted Date
- 2024-06-14
- Last Posted Date
- 2025-06-22
- Lead Sponsor
- Institut Curie
- Target Recruit Count
- 110
- Registration Number
- NCT06459791
- Locations
- 🇫🇷
Institut Curie, Saint-Cloud, France
🇫🇷Hôpital Saint-Louis - AP-HP Senopole, Paris, France
Optimizing Bronchopulmonary Cancer Screening
- Conditions
- Diagnoses DiseaseBronchopulmonary Disease
- First Posted Date
- 2024-06-03
- Last Posted Date
- 2025-02-03
- Lead Sponsor
- Institut Curie
- Target Recruit Count
- 500
- Registration Number
- NCT06439901
- Locations
- 🇫🇷
Centre CTPS Bobigny Bondy, Bobigny, France
🇫🇷Centre Municipal de Santé Simone Veil, Issy-les-Moulineaux, France
🇫🇷Centre Municipal de Santé Jacqueline Akoun-Cornet, Malakoff, France
68Ga-FAPI-46 PET/CT for Predicting Histological Response in Triple-negative Breast Cancer (FAP-IT)
- Conditions
- Triple Negative Breast Cancer
- First Posted Date
- 2024-04-05
- Last Posted Date
- 2025-07-01
- Lead Sponsor
- Institut Curie
- Target Recruit Count
- 60
- Registration Number
- NCT06349512
- Locations
- 🇫🇷
Hôpital Privé d'Antony, Antony, France
🇫🇷Institut Curie -site Paris, Paris, France
🇫🇷GH Diaconesses Croix Saint-Simon, Paris, France
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News
Egle Therapeutics Secures €9.3 Million in French Government Funding to Advance Treg-Targeting Cancer Therapies
Egle Therapeutics has received €9.3 million in non-dilutive funding from France 2030's "Innovations in Biotherapies and Bioproduction" initiative to accelerate development of its lead immuno-oncology candidate EGL-001.
Distinct Mechanisms of HER2-Targeting Agents in NSCLC: Understanding TKIs vs ADCs
• TKIs target the intracellular kinase domain of HER2, inhibiting cell proliferation pathways, while ADCs utilize antibodies to deliver cytotoxic payloads directly to cancer cells. • HER2-directed ADCs demonstrate broader efficacy across various HER2 alterations, including mutations, amplifications, and overexpression, offering versatile treatment options. • TKIs offer advantages of oral administration and established safety profiles, though their effectiveness can vary depending on specific HER2 mutations in the ATP binding domain.
Valerio Therapeutics Expands Antibody Development Capabilities with Emglev Therapeutics Acquisition
Valerio Therapeutics has acquired Emglev Therapeutics, gaining access to innovative single-domain antibody (sdAb) technology that enables fully human antibody development through in vitro processes.
VESPER Trial: BaSq Subtype Linked to Poorer Outcomes in Bladder Cancer
The VESPER trial's molecular subtyping analysis reveals the BaSq subtype (pure or mixed) is associated with decreased progression-free survival and overall survival in bladder cancer patients.
Telisotuzumab Vedotin Improves Patient-Reported Outcomes in c-Met+ NSCLC
• The LUMINOSITY trial showed telisotuzumab vedotin (Teliso-V) yielded a 29% response rate in patients with c-Met-overexpressing, EGFR wild-type, nonsquamous NSCLC. • Patient-reported outcomes from LUMINOSITY indicated improvements in key cancer-related symptoms like cough and chest pain with Teliso-V treatment. • The trial also demonstrated that Teliso-V maintained quality of life and physical functioning, particularly in patients achieving disease control. • Peripheral neuropathy, a notable side effect, was reported by patients, highlighting the need for proactive management in subsequent trials.