Studies
Gelukkig staat de wetenschap niet stil en wordt er in de geneeskunde dagelijks vooruitgang geboekt. De dienst longziekten van AZ-Delta tracht ook hier een actieve rol te spelen oa. door deelname aan een waaier van klinische studies.
Dergelijke klinische studies lopen er momenteel in het domein van oa. astma, COPD, longkanker, IPF en chronische hoest. Samen met uw huisarts en longarts wordt u de gelegenheid geboden om aan dergelijke studie deel te nemen. Uiteraard is uw deelname volledig vrijblijvend. Een besluit om al dan niet deel te nemen kan slechts worden genomen na voldoende te zijn geinformeerd. Uw longarts en studie-coördinator zullen antwoorden op al uw vragen.
Aarzel niet om contact met ons op te nemen.
- Voor respiratoire oncologie via
- 051 / 23 72 07 - melissa.masschelin@azdelta.be (Melissa)
- 051 / 23 75 04 - Lore.carton@azdelta.be (Lore)
- Voor COPD, astma, chronische hoest en IPF via
- 051 / 23 76 18 - mathijs.bonne@azdelta.be (Mathijs)
- 051 / 23 73 95 - jessy.meirsman@azdelta.be (Jessy)
Klinische studies longkanker AZ Delta – maart 2026
SCLC - small cell lung cancer
Non-metastatic
Currently no open trials
Metastatic
First line
Currently no open trials
Second line
IDeate-Lung02 (Daichi Sankyo) (DS7300-188)
A phase 3, multicenter, randomized,open-label study of ifinatamab deruxtecan (idxd), a b7-h3 antibody-drug conjugate (adc), versus treatment of physician’s choice (topotecan) in subjects with relapsed small cell lung cancer
EVOKE-SCLC-04 (Gilead)
A Global, Multicenter, Randomized, Open-label, Phase 3 Study of Sacituzumab Govitecan (antibody-drug conjugate targeting TROP2) Versus Standard of Care (SOC) in Participants With PreviouslyTreated Extensive Stage Small Cell Lung Cancer (ES-SCLC)
NSCLC non-metastatic
Resectable
Neo-coast2 (Astra Zeneca)
A Phase II, Open-label, Multicentre, Randomised Study of Neoadjuvant and Adjuvant Treatment in Patients with Resectable, Early-stage (II to IIIB) Non-small Cell Lung Cancer
KRASG12c + NSCLC: SUNRAY-02 (Lilly)
A Phase 3, Multicenter, Double-Blind, Placebo-controlled Study Assessing the Efficacy and Safety of Olomorasib in Combination with Standard of Care Immunotherapy in Pts with Resected or Unresectable KRAS G12C-Mutant, NSCLC (JZQH)
Unresectable
SUNRAY-02 (Lilly) : open September 2026
A Phase 3, Multicenter, Double-Blind, Placebo-controlled Study Assessing the Efficacy and Safety of Olomorasib in Combination with Standard of Care Immunotherapy in Pts with Resected or Unresectable KRAS G12C-Mutant, NSCLC (JZQH)
NSCLC metastatic-no molecular target
1st line
Squamous and non-squamous
Artemide (Astra Zeneca)
A Phase III, Randomized, Double-blind, Multicenter, Global Study of Rilvegostomig (bispecific antibody, anti PDL1 en anti-TIGIT) or Pembrolizumab Monotherapy for the First-line Treatment of Patients with PD-L1-high Metastatic Non-small Cell Lung Cancer
Rosetta Lung-02 (Biontech): open August 2026
A Phase II/III, multisite, randomized master protocol for a global trial of Pumitamig (bispecific antibody, anti PDL1 en anti-VEGF) in combination with chemotherapy and other investigational agents in first-line non-small cell lung cancer
Non-squamous
Relativity CA224-1093 (BMS)
A Phase 3, Randomized, open-label Study of Nivolumab + Relatlimab (anti-LAG-3) Fixed-dose Combination with Chemotherapy Versus Pembrolizumab with Chemotherapy as First-line Treatment for Participants with Non-squamous (NSQ), Stage IV or Recurrent Nonsmall Cell Lung Cancer and with Tumor Cell PD-L1 Expression ≥ 1%
AndroMETa M24-536 (ABBVIE): part 2 open end of 2025
An Open-label Multi-Cohort Phase 1b/2 Study to Evaluate the Safety, Efficacy, and Optimal Dose of ABBV-400 (telisotuzumab adizutecan, c-Met-targeting antibody-drug conjugate) in Combination with Budigalimab (anti-PD1) in Advanced or Metastatic Non-Squamous NSCLC with No Prior Treatment for Advanced Disease and No Actionable Genomic Alterations (AndroMETa-Lung-536)
Pulse: maintenance (academic)
Maintenance Pembrolizumab at usual or low dose non-squamous lung cancer: a non-inferiority study.
2nd + line
Artemia (OSE Immunotherapeutics)
A randomized, open-label, phase 3 trial comparing the efficacy and safety of OSE2101 (Tedopi®) versus docetaxel in HLA-A2 positive patients with metastatic NonSmall Cell Lung Cancer (NSCLC) and secondary resistance to Immune Checkpoint Inhibitors (ICI)
RAINFOL-05 (GCT1184-05 , Genmab)
A Phase 2, Open-label, Multicohort Study of Rinatabart Sesutecan (antibody-drug conjugate targeting folate receptor alpha) in Participants with Non-Small Cell Lung Cancer.
NSCLC metastatic-molecular target
All actionable genomic alteration
(ie, ALK, RET, ROS1 rearrangement, KRAS G12C, BRAF mutations, and MET exon 14 skipping mutations/MET,amplification, and HER2 mutations)
2nd + line
RAINFOL-05 (GCT1184-05 , Genmab)
A Phase 2, Open-label, Multicohort Study of Rinatabart Sesutecan (antibody-drug conjugate targeting folate receptor alpha) in Participants with Non-Small Cell Lung Cancer.
EGFR common exon 19 or exon 21 mutation
1st line
LAT-FLOSI (Academic)
LAT (Local ablative therapy) for Oligoprogressive NSCLC Treated With First-line OSImertinib (LATFLOSI).
2nd + line
TROPION-LUNG15 (Astra Zeneca)
A Study to Investigate the Efficacy and Safety of Dato-DXd (Datopotamab deruxtecan, antibody-drug conjugate targeting TROP2) With or Without Osimertinib Compared With Platinum Based Doublet Chemotherapy in Participants With EGFR-Mutated Locally Advanced or Metastatic Non-Small Cell Lung Cancer
RAINFOL-05 (GCT1184-05 , Genmab)
A Phase 2, Open-label, Multicohort Study of Rinatabart Sesutecan (antibody-drug conjugate targeting folate receptor alpha) in Participants with Non-Small Cell Lung Cancer.
EGFR exon 20 insertion mutation
1st line
Currently no open trials
2nd + line
RAINFOL-05 (GCT1184-05 , Genmab)
A Phase 2, Open-label, Multicohort Study of Rinatabart Sesutecan (antibody-drug conjugate targeting folate receptor alpha) in Participants with Non-Small Cell Lung Cancer.
HER2 mutation
1st line
SOHO-2 Bayer
A Phase 3 Open-label, Randomized, Active-controlled, Multicenter Trial to Evaluate the Efficacy and Safety of Orally Administered sevabertinib (BAY 2927088) Compared With Standard of Care as a First-line Therapy in Patients With Locally Advanced or Metastatic NSCLC With HER2-activating Mutations.
MET exon 14 skipping mutation
Currently no open trials
(K)RAS mutation
1st line
KRASCENDO 170 (Roche): cohortes C & D open April 2026
Phase Ib/II, open-label, multicenter study evaluating the safety, activity, and pharmacokinetics of divarasib in combination with other anti-cancer therapies in patients with previously untreated advanced or metastatic non-small cell lung cancer with a kras g12c mutation
Currently no cohorts open
Krascendo2 (Roche)
A Study Evaluating the Efficacy and Safety of Divarasib and Pembrolizumab Versus Pembrolizumab and Pemetrexed and Carboplatin or Cisplatin in Participants With Previously Untreated, KRAS G12C-Mutated, Advanced or Metastatic Non-Squamous Non-Small Cell Lung Cancer (Krascendo 2)
2nd + line
All RAS mutations
RASolve 301 (RMC-6236-301, Revolution Medicine)
Phase 3 Multicenter, Open Label, Randomized Study of daraxonrasib (RMC-6236) Versus Docetaxel in Patients With Previously Treated Locally Advanced or Metastatic RAS[MUT] NSCLC
RAINFOL-05 (GCT1184-05 , Genmab)
A Phase 2, Open-label, Multicohort Study of Rinatabart Sesutecan (antibody-drug conjugate targeting folate receptor alpha) in Participants with Non-Small Cell Lung Cancer.
ALK fusion
1st line
Currently no open trials
2nd + line
RAINFOL-05 (GCT1184-05 , Genmab)
A Phase 2, Open-label, Multicohort Study of Rinatabart Sesutecan (antibody-drug conjugate targeting folate receptor alpha) in Participants with Non-Small Cell Lung Cancer.
BRAF mutation
1st line
Currently no open trials
2nd + line
RAINFOL-05 (GCT1184-05 , Genmab)
A Phase 2, Open-label, Multicohort Study of Rinatabart Sesutecan (antibody-drug conjugate targeting folate receptor alpha) in Participants with Non-Small Cell Lung Cancer.
Other trials
Currently no other open trials
Recently closed
Delphi 312 (Amgen)
A Phase 3, Open Label, Multicenter, Randomized Study of First Line Tarlatamab in combination with Durvalumab, Carboplatin and Etoposide versus Durvalumab, Carboplatin and Etoposide in Untreated Extensive Stage Small-Cell Lung Cancer (DeLLphi-312)
REZILIENT 3 (Taiho Oncology)
Randomized, Controlled, Open-label, Phase 3, Global MultiCenter Trial to Assess the Efficacy and Safety of Zipalertinib plus Chemotherapy versus Chemotherapy alone, in Patients with Previously Untreated, Locally Advanced or Metastatic Nonsquamous Non-Small Cell Lung Cancer (NSCLC) with Epidermal Growth Factor Receptor (EGFR) Exon 20 Insertion (ex20ins) Mutations
IPF – Idiopathic Pulmonary Fibrosis
Currently no open trials
COPD
The effect of home-based inspiratory muscle training compared to usual care on readmission rate in patients after a severe acute exacerbation of chronic obstructive pulmonary disease: a randomised, multicentre, parallel group clinical trial: IN-SPIRED trial.
Asthma
Currently no open trials
Chronic cough
ASPIRE
A Phase 2b, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy, Safety, and Tolerability of Taplucainium Inhalation Powder (NOC-110) in Adults with Refractory or Unexplained Chronic Cough.
Lees meer...Inclusion criteria:
- 18-80 years of age
- Have had a chronic cough for at least 1 year
- Have seen a doctor and received prescribed or over-the-counter medicines but without improvement
- 24-hour cough frequency of ≥20 per hour
Exclusion criteria:
- Current smoker/vaper or individuals who have given up smoking within the past 6 months
- Body Mass Index of ≥40 kg/m2
- Supine systolic blood pressure >150 mmHg or <85 mmHg, a supine diastolic blood pressure >95 mmHg or <40 mmHg, or a pulse rate ≥100 or <40 beats per minute
- Diagnosis of COPD or other pulmonary diseases
Excluded medications:
- Opioids (e.g. morphine)
- Gabapentin (tricyclics)
- Chronic, systemic corticosteroid use
- Inhalers
- Medication to aid sleep
- Medication to regulate blood pressure (e.g. Losartan)
- Cough suppressant (e.g. paracodine)
- Speech therapy
Other
TILIA
A Phase III, Multicentre, Randomised, Double-blind, Parallel-group, Placebo-controlled Study to Evaluate the Efficacy and Safety of Tozorakimab (MEDI3506) in Patients Hospitalised for Viral Lung Infection Requiring Supplemental Oxygen (TILIA)
Lees meer...- Adult participants ≥ 18 years old at the time of signing the ICF.
- Patients hospitalised with viral lung infection. Note: Suspected viral aetiology is
- acceptable to meet this criterion.
- Hypoxaemia requiring treatment with supplemental O2, consistent with WHO Clinical
- Progression Scale for Disease Progression score of 5 and 6.
- Note: Hypoxemia is defined as SpO2 ≤ 94% on room air at screening, or documented
- SpO2 ≤ 94% prior to initiation of oxygen therapy. Patients receiving oxygen > 6 L/min
- or non-invasive ventilation will be considered to have met this inclusion criterion
- regardless of SpO2 levels.
- ≤ 36 hours since admission to hospital.
- ≤ 14 days since onset of respiratory viral infection symptoms.