Hedgehog Inhibition for Pancreatic Ductal Adenocarcinoma (PDAC) in the Preoperative Setting (HIPPoS)

Pancreatic Ductal Adenocarcinoma Clinical Trial

— HIPPoS  

Official title:

Proof of Mechanism Study of an Oral Hedgehog Inhibitor (GDC-0449) in Patients With Resectable Pancreatic Ductal Adenocarcinoma in the Pre-operative Window Period

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01096732
• Other study ID #: OCRD 201014
• Status: Terminated
• Phase: Phase 2
• First received: March 30, 2010
• Last updated: January 7, 2014
• Start date: February 2011
• Est. completion date: August 2012

Study information

• Verified date: January 2014
• Source: Cambridge University Hospitals NHS Foundation Trust
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency
• Study type: Interventional

Clinical Trial Summary

This clinical trial is looking at the effect of a new drug called GDC-0449 in patients with cancer of the pancreas. Laboratory studies have shown that this drug blocks a process in pancreatic cells thought to be involved in cancer development and spread. This process is called the 'Hedgehog signalling pathway'. As yet, it is unclear whether blocking hedgehog signalling will directly affect the tumour cells themselves or the surrounding normal tissue. Understanding this distinction will help improve treatment strategies for pancreatic cancer. Patients will be offered to participate in this research study if they have localised pancreatic cancer that can be removed by surgery. In the period between diagnosis and surgery the investigators do not normally treat patients, however in this trial the investigators will ask patients to take GDC-0449 during the approximately two weeks until the day of surgery. All patients that enter this study will have undergone a diagnostic biopsy of the pancreatic tumour and the investigators will collect a second sample of the tumour at surgery. The main question of this study is whether the investigators can detect a change in hedgehog signalling in the normal tumour surrounding tissue. Furthermore the investigators will look very carefully whether this treatment is safe for patients. All problems before and after surgery will be carefully documented and the investigators have defined strict rules to stop the study if the investigators observe serious problems.

Description:

Please contact Principal Investigators team for full details.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 3
• Est. completion date: August 2012
• Est. primary completion date: August 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Documented tissue diagnosis of pancreatic ductal adenocarcinoma with a sufficient amount of tissue for Laser Capture Micro-dissection (LCM) of the stromal and tumour compartments.

• Confirmed eligibility for a Whipple's or distal pancreatectomy procedure by Multi-Disciplinary Team (MDT) and surgeon review.

• Adequate organ function defined as:

• Creatinine clearance = 50ml/min (as defined by Cockcroft-Gault)

• Electrolytes (Sodium (Na)/Potassium (K)/Calcium (Ca)) within institutional normal limits

• Alanine transaminase (ALT)/Aspartate transaminase (AST) <5*ULN

• Partial thromboplastin time (PTT)<2*ULN, prior supplementation with vitamin K is allowed

• Adequate blood counts: neutrophils >1,500/µl, Hb > 6mmol/L,platelets >100.000/µl

• Albumin = 25mg/dL

• Written informed consent

• Male or female aged 18 years or over.

• World Health Organization (WHO) performance status 0-1

• Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests, and other study procedures.

• Males should not donate sperm during treatment or up to 3 months after the last dose.

• Women of childbearing potential are required to have a negative serum pregnancy test (with sensitivity of at least 25 mIU/mL) within 10-14 days and within 24 hours prior to the first dose of GDC-0449.

Exclusion Criteria:

• Known Hepatitis B/C or Human Immunodeficiency Virus (HIV) infection

• Known hypersensitivity to GDC-0449

• Active cardiac ischemic disease (this criterion only applies for participation in the imaging part of the study)

• Women, who are pregnant plan to become pregnant or are lactating (during the study or for up to 12 months after the last dose).

• Concurrent participation in another clinical trial using an investigational medicinal product.

• Other severe acute or chronic medical or psychiatric condition, or laboratory abnormality that may increase the risk associated with study participation or study drug administration, or in the judgment of the investigator would make it undesirable for the patient to enter the trial (i.e. patients is not able to swallow tablets).

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Adenocarcinoma
• Pancreatic Ductal Adenocarcinoma

Intervention

Drug:
• GDC-0449
Gelatine capsules of 150mg.Taken O.D. for 14 days.

Locations

Country	Name	City	State
United Kingdom	Cambridge University Hospitals NHS Foundation Trust	Cambridge

Sponsors (3)

Lead Sponsor	Collaborator
Lisa Bax	Genentech, Inc., Roche Pharma AG

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To study the effect of GDC-0449 treatment on the stromal cell and tumour cell hedgehog signalling in patients with Pancreatic Ductal Adenocarcinoma.	To study the effect of GDC-0449 treatment on the stromal cell and tumour cell hedgehog signalling in patients with Pancreatic Ductal Adenocarcinoma.; To study the safety and tolerability of pre-operative GDC-0449 treatment in patients who undergo Whipple's or distal pancreatectomy surgery for Pancreatic Ductal Adenocarcinoma.	18 months	Yes