Study of Milciclib in Patients With Unresectable/Metastatic Hepatocellular Carcinoma

NCT03109886 | Completed Phase 2 DMC

• 2 other identifiers: CDKO-125a-0102017-000144-18
• Study Type: interventional
• Target: 31
• Locations: 3 countries
• Sites: 14

Brief Summary

The primary aim of this exploratory study is to test the safety and tolerability of milciclib when administered orally at 100 mg in patients with recurrent or metastatic Hepatocellular Carcinoma. The evaluation of the efficacy profile is a secondary objective of the study. Moreover, markers expression in tumor cells and plasma will be studied and described in association with the clinical outcome. Eligible patients will receive milciclib orally on a daily schedule for 4 consecutive days a week in a 4-week cycle (4 days on/3 days off x q4 wks) for a total of 12 weeks (i.e. 3 cycles) unless patient refusal, consent withdrawal, Investigator's decision, unacceptable toxicity or death whichever occurs earlier. At the end of Cycle 3, treatment will be stopped, and based on the results of the tumor assessment performed on Day 90 (±3 days) from treatment start, patients will be followed as here below detailed:

• patients with Complete Response (CR)/Partial Response (PR)/Stable Disease (SD) will be followed for safety until 30 days from last dose intake (or until a new anticancer therapy starts, whichever occurs earlier) and will be assessed for efficacy in the follow-up period up to Day 180 from treatment start;
• patients with progressive disease will be followed only for safety until 30 days from last dose intake (or until a new anticancer therapy starts, whichever occurs earlier). After the completion of three cycles, patients who, in the Investigator's judgment, are benefiting from treatment with milciclib, will resume treatment and will remain on study up to Day 180 from treatment start, unless withdrawal criteria are met earlier.

Conditions

Hepatocellular Carcinoma

Keywords

Unresectable Hepatocellular Carcinoma; Metastatic Hepatocellular Carcinoma; Child-Pugh Class A

Outcome Measures

Primary Outcomes (1)

• Overall Safety Profile

  Overall safety profile, evaluated on the basis of laboratory (i.e. hematology and blood chemistry, urinalysis, vital signs, ophthalmologic examinations) and adverse events emerging during the trial, will be determined. The National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version 4.03 will be used for the severity grading of adverse events and of hematological and blood chemistry abnormalities

  From Informed Consent signature to 30 days after last dose intake up to Day 180 from treatment start

Secondary Outcomes (6)

• Objective Response Rate (ORR)

  At screening; During treatment at Day 45 and 90; During follow up at Day 180 for patients not progressed at previous assessments

• Objective Response Rate (ORR)

  At screening; During treatment at Day 45 and 90; During follow up at Day 180 for patients not progressed at previous assessments

• Progression-Free Survival (PFS)

  From treatment start to date of progression assessed on Day 45, 90 or 180 or to date of death if before day 180

• Time to Progression (TPP)

  From treatment start to date of progression assessed on Day 45, 90 or 180 or to date of death if before day 180

• TPP-3 months

  Based on tumor assessment at or after 3 months from treatment start

Study Arms (1)

Milciclib maleate

EXPERIMENTAL

milciclib maleate ,10, 50 and 100 mg hard gelatine capsules , 100 mg once daily, for 4 consecutive days a week in a 4-week cycle (4 days on/3 days off x q4 wks) for a total of 12 weeks (i.e. 3 cycles)

Drug: Milciclib maleate

Interventions

Milciclib maleate DRUG

100 mg/day once daily, for 4 consecutive days a week in a 4-week cycle (4 days on/3 days off x q4 wks) for a total of 12 weeks (i.e. 3 cycles) unless patient refusal, consent withdrawal, Investigator's decision, unacceptable toxicity or death whichever occurs earlier. After the completion of three cycles, patients who, in the Investigator's judgment, are benefiting from treatment with milciclib, will resume treatment and will remain on study up to Day 180 from treatment start, unless withdrawal criteria are met earlier.

Also known as: PHA-848125AC

Milciclib maleate

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients with diagnosis of HCC, confirmed by histology or radiology according to American Association for the Study of Liver Diseases/European Association for the Study of the Liver (AASLD/EASL) criteria prior to the start of the investigational product. Imaging characteristics should be retrieved from at least a 3-phase liver protocol CT or MRI with target tumor lesion(s) demonstrating arterial hyper-enhancement and wash-out in the venous phase;
• Tumor stages eligible for the study are defined as:
• HCC within the Barcelona Clinic Liver Cancer (BCLC) stage C. In case of portal vein thrombosis (PVT) an associated target lesion in the liver parenchyma should be clearly defined. PVT without associated target lesion are not eligible to the study;
• Untreatable post-chemoembolization (TACE) or post-radioembolization (TARE) progression defined as BCLC stage B or C with radiographic progression according to mRECIST after TACE or TARE not eligible for further surgical or loco-regional therapy;
• Recurring HCC non eligible for pre-transplant downstaging protocols or for resection;
• Patients must have failed sorafenib treatment or be intolerant to sorafenib or actively refusing sorafenib
• Failing sorafenib treatment is defined if after ≥ 14 days of therapy (not necessarily consecutive) radiology progression is ascertained according to mRECIST;
• Intolerant to sorafenib treatment is defined as a sorafenib related Grade 2 or greater adverse event (CTC-AE) that continues or recurs after sorafenib treatment interruption for 7 days or dose reduction;
• Active refusal should be documented by a written and signed patient declaration to be filed in the clinical records;
• Child-Pugh score ≤ 6 (class A);
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1;
• Local or loco-regional therapy (i.e., surgery, radiation therapy, hepatic arterial embolization, chemoembolization, radioembolization, radiofrequency ablation, percutaneous ethanol injection, or cryoablation) must have been completed ≥4 weeks prior to study entry with documentation of progressive or recurrent disease;
• Signed and dated Investigational Review Board/Independent Ethics Committee (IRB/IEC) approved Informed Consent/Genetic Consent.

You may not qualify if:

• Prior use of any systemic anti-cancer therapy (including experimental agents and immunotherapy) except for sorafenib and second line treatment with regorafenib discontinued for intolerance within 14 days;
• Known fibrolamellar HCC or mixed hepato-cholangiocarcinoma;
• Grade 3 oesophageal varices, regardless of previous bleeding episodes on endoscopy performed no more than in the last 12 months;
• Clinical meaningful ascites defined as CTCAE Grade≥2. Patient who have been on a stable medication regimen for at least 2 months to manage ascites are eligible if they show no ascites at the clinical examination. Patients with clinically undetectable ascites who are Child A with detectable ascites at CT/MRI are eligible to the protocol;

Sponsors & Collaborators

• Tiziana Life Sciences LTD: lead

Study Sites (14)

Ippokrateio General Hospital of Athens

Athens, 11527, Greece

Location

Laiko General Hospital of Athens

Athens, 11527, Greece

Location

General University Hospital of Larissa

Larissa, 41110, Greece

Location

University General Hospital of Thessaloniki - AHEPA

Thessaloniki, 54636, Greece

Location

Rambam Health Corporation

Haifa, 31096, Israel

Location

Rabin Medical Center - Beilinson Hospital

Petah Tikva, 4941492, Israel

Location

The Sheba Academic Medical Center Hospital - Tel Hashomer

Ramat Gan, Israel

Location

Tel Aviv Sourasky Medical Center

Tel Aviv, 64239, Israel

Location

Istituto Clinico Humanitas

Rozzano, MI, 20089, Italy

Location

AOU S. Orsola Malpighi Bologna

Bologna, 40138, Italy

Location

Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico

Milan, 20122, Italy

Location

Azienda Ospedaliera Universitaria Policlinico di Modena

Modena, 41124, Italy

Location

A.O.U. Federico II

Napoli, 80131, Italy

Location

A.O. U. Policlinico Paolo Giaccone

Palermo, 90127, Italy

Location

MeSH Terms

Conditions

Carcinoma, Hepatocellular

Interventions

N,1,4,4-tetramethyl-8-((4-(4-methylpiperazin-1-yl)phenyl)amino)-4,5-dihydro-1H-pyrazolo(4,3-h)quinazoline-3-carboxamide

Condition Hierarchy (Ancestors)

Adenocarcinoma; Carcinoma; Neoplasms, Glandular and Epithelial; Neoplasms by Histologic Type; Neoplasms; Liver Neoplasms; Digestive System Neoplasms; Neoplasms by Site; Digestive System Diseases; Liver Diseases

Study Officials

• Fayez M Hamzeh, MD

  Tiziana Life Sciences LTD

  STUDY CHAIR

• Angelo Sangiovanni, MD, PHD

  Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico - Milano, Italy

  PRINCIPAL INVESTIGATOR

• Armando Santoro, MD

  Istituto Clinico Humanitas - Rozzano (MI), Italy

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 30, 2017
• First Posted: April 12, 2017
• Study Start: July 12, 2017
• Primary Completion: May 16, 2019
• Study Completion: June 20, 2019
• Last Updated: October 12, 2021

Record last verified: 2021-10

Data Sharing

• IPD Sharing: Will not share

Locations

GR (4); IT (6); IL (4)