Clinical trials

4

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Magnetic Resonance Imaging (MRI) Guided Stereotactic Adaptive Radiotherapy for Targeting Abdominal Cancer

The aim of this study is to investigate the effect of MRI-guided adaptive stereotactic radiotherapy on local control, survival, and toxicity in the treatment of oligometastatic cancer to the abdomen.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Australasian Gastro-Intestinal Trials GroupUpdated: May 8, 2026Locations: 2
Eligibility criteria

Aged 18 years or older [+16]

Contra-indication to MRI [+6]

Status: Recruiting

Phase II Study of the Combination of Durvalumab (MEDI4736) (PDL1 Inhibitor) and Olaparib (PARP Inhibitor) in Advanced Cholangiocarcinoma After Initial Chemotherapy and Durvalumab (BIL-PPP)

The aim of this study is to investigate whether the combination of durvalumab and olaparib in the maintenance setting after initial chemotherapy and durvalumab will benefit patients with locally advanced or metastatic cholangiocarcinoma.

Participants needed: 40
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Australasian Gastro-Intestinal Trials GroupUpdated: May 6, 2026Locations: 8
Eligibility criteria

Age ≥18 years, and life expectancy>12 weeks [+16]

Previous use of a PARP inhibitor. [+30]

Status: Recruiting

A Trial of Palliative Chemotherapy, Radiation and Immune Treatment for Oesophageal Cancer: PALEO Study

The purpose of this study is to investigate the effects of the addition of the stereotactic body radiotherapy and durvalumab to a well tolerated 2 week chemotherapy and radiation treatment regimen in people with esophageal cancer that is locally advanced or has spread to another area of the body (metastasized).

Participants needed: 54
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Australasian Gastro-Intestinal Trials GroupUpdated: May 8, 2026Locations: 9
Eligibility criteria

Males and females > 18 years of age. [+20]

Bulky or organ-threatening metastatic disease requiring upfront higher dose chem... [+24]

Status: Recruiting

Cessation of Somatostatin Analogues After PRRT in Mid, Hind-Gut and Pancreatic Neuroendocrine Tumours

Neuroendocrine tumours (NETs) are slow growing cancers, which commonly present as metastatic incurable disease. Some neuroendocrine tumours, termed functional NETs, overproduce hormones which result in a variety of symptoms. However, approximately 75% of NETs are considered non-functional meaning that they do not result in hormone overproduction. The main treatment for both functional and non-functional NETs is somatostatin analogues (SSA, a type of inhibitory hormone). These drugs slow tumour growth and reduce hormone production. Over time, the majority of patients will experience tumour growth despite treatment with SSA therapy. When this occurs, the addition of Peptide Receptor Radionuclide Therapy (PRRT, a type of targeted radiotherapy) in combination with ongoing SSA therapy is given. However, it is not known if continuing SSA therapy after commencement of PRRT is beneficial or not. The aim of this study is to estimate the outcomes of patients with grade 1 and 2 well differentiated mid, hind-gut or pancreatic neuroendocrine tumours who have progressed on SSA therapy and receive subsequent PRRT with or without concurrent SSA.

Participants needed: 78
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Australasian Gastro-Intestinal Trials GroupUpdated: Aug 14, 2025Locations: 12
Eligibility criteria

Adults over 18 years of age with well or moderately differentiated mid or hindgu... [+15]

This study is for pancreatic, mid-gut and hind-gut NET only. Gastric and lung NE... [+9]