A Study of Efficacy and Safety of Fruquintinib (HMPL-013) in Participants With Metastatic Colorectal Cancer (FRESCO-2)

A Global Multicenter Randomized Placebo-Controlled Phase 3 Trial To Compare The Efficacy And Safety Of Fruquintinib Plus Best Supportive Care To Placebo Plus Best Supportive Care In Patients With Refractory Metastatic Colorectal Cancer

This is a global, randomized, double-blind, placebo-controlled, multicenter phase 3 clinical trial to compare the efficacy and safety of fruquintinib plus best supportive care (BSC) versus placebo plus BSC in participants with refractory metastatic colorectal cancer (mCRC). 691 participants were randomized to one of the following treatment arms in a 2:1 ratio, fruquintinib plus BSC or placebo plus BSC.

Study Overview

• Status: Active, not recruiting
• Conditions: Metastatic Colorectal Cancer; Metastatic Colon Cancer
• Intervention / Treatment: Drug: Fruquintinib; Drug: Placebo

Detailed Description

This is a global, randomized, double-blind, placebo-controlled, multicenter phase 3 clinical trial to compare the efficacy and safety of fruquintinib in combination with BSC versus placebo in combination with BSC in metastatic colorectal cancer participants who have progressed on, or were intolerant to, chemotherapy, anti-VEGF and anti-EGFR biologics, and TAS-102 or regorafenib. Participants with MSI-H/MMR deficient tumors must have also received an immune checkpoint inhibitor if approved and available and if deemed appropriate. Subjects with BRAF-mutant tumors must have been treated with a BRAF inhibitor if approved and available and if deemed appropriate.

Metastatic colorectal cancer cannot be cured by surgery. Therefore, treatment principals are primarily aimed at controlling disease progression and prolonging survival. Standard first- and second-line therapy includes cytotoxic drugs such as 5-fluorouracil, oxaliplatin, and irinotecan; anti-VEGF therapy; and, if RAS wild type, anti-EGFR therapy. After the first two lines of chemotherapy, standard third-line treatment is either TAS-102 or regorafenib. There are currently no effective treatments for patients who have progressed on standard, approved therapies, and treatment options include reuse of prior therapies, clinical trials or BSC. Consequently, there is an unmet medical need for additional safe and effective treatment.

• Study Type: Interventional
• Enrollment (Actual): 691
• Phase: Phase 3

Contacts and Locations

Study Locations

• Australia
  • Queensland
    • Brisbane, Queensland, Australia, 4001
      • Integrated Clinical Oncology Network Pty Ltd (ICON)
  • South Australia
    • Adelaide, South Australia, Australia, 5011
      • The Queen Elizabeth Hospital
    • Adelaide, South Australia, Australia, 5042
      • Flinders Medical Centre
  • Victoria
    • Melbourne, Victoria, Australia, 3021
      • Western Health
    • Melbourne, Victoria, Australia, 3084
      • Austin Hopistal Medical Oncology Unit
    • Melbourne, Victoria, Australia, 3168
      • Monash Health
• Austria
  • AUT
    • Linz, AUT, Austria, 4010
      • Ordensklinikum Linz Barmherzige Schwestern
    • Rankweil, AUT, Austria, 6830
      • Schwerpunktkrankenhaus Feldkirch
    • Steyr, AUT, Austria, 4400
      • Klinikum Steyr
    • Wels, AUT, Austria, 4600
      • Klinikum Wels-Grieskirchen GmbH
    • Wien, AUT, Austria, 1160
      • Wiener Gesundheitsverbund - Klinik Ottakring
    • Wiener Neustadt, AUT, Austria, 2700
      • Landesklinikum Wiener Neustadt
• Belgium
  • BEL
    • Aalst, BEL, Belgium, 9300
      • Onze-Lieve-Vrouwziekenhuis OLV - Campus Aalst
    • Brussels, BEL, Belgium, 1200
      • UCL St-Luc
    • Charleroi, BEL, Belgium, 6000
      • Grand Hopital de Charleroi
    • Edegem, BEL, Belgium, 2650
      • UZ Antwerpen
    • Haine-Saint-Paul, BEL, Belgium, 7100
      • Centres Hospitaliers Jolimont
    • Leuven, BEL, Belgium, 3000
      • UZ Leuven
    • Roeselare, BEL, Belgium, 8800
      • AZ Delta Roeselare
    • Turnhout, BEL, Belgium, 2300
      • AZ Turnhout
    • Yvoir, BEL, Belgium, 5530
      • CHU Mont-Godinne
  • Wallonia
    • Liège, Wallonia, Belgium, 4000
      • Clinique CHC MontLégia
    • Liège, Wallonia, Belgium, 4001
      • CHU de Lige - Domaine Universitaire du Sart Tilman
• Czechia
  • Prague, Czechia, 12808
    • Vseobecna Fakultni Nemocnice VFN, Onkologicka Klinika
  • Moravia
    • Brno, Moravia, Czechia, 60200
      • Masaryk Memorial Cancer Institute, Hematoonkologie
    • Olomouc, Moravia, Czechia, 77900
      • Fakultni nemocnice Olomouc, Onkologicka klinika
• Estonia
  • Tartu, Estonia, 50406
    • Tartu University Hospital Clinic of Haematology and Oncology
  • Harju
    • Tallinn, Harju, Estonia, 11312
      • East Tallinn Central Hospital Centre of Oncology
    • Tallinn, Harju, Estonia, 13419
      • Sihtasutus Pohja-Eesti Regionaalhaigla (PERH) (North Estonia Medical Centre)
• France
  • FRA
    • Bordeaux, FRA, France, 33000
      • Institut Bergonie
    • Caen, FRA, France, 14000
      • UNICANCER
    • Dijon, FRA, France, 21000
      • Centre Georges-François Leclerc
    • Montpellier, FRA, France, 34298
      • ICM-Val d'Aurelle
    • Paris, FRA, France, 75010
      • Saint-Louis Hospital
    • Paris, FRA, France, 75012
      • Hopital St Antoine
    • Paris, FRA, France, 75013
      • Hopital Pitie Salptriere
    • Poitiers, FRA, France, 86000
      • CHU Poitiers
    • Pringy, FRA, France, 74370
      • Centre Hospitalier Annecy Genevois
    • Rennes, FRA, France, 35033
      • Centre Hospitalier Universitaire CHU de Rennes - Hopital de Pontchaillou
    • Strasbourg, FRA, France, 67033
      • Institut de Cancérologie Strasbourg-Europe
  • Franche-Comte
    • Besançon, Franche-Comte, France, 25000
      • CHU Besançon
  • Paris
    • Villejuif, Paris, France, 94805
      • Institut Gustave Roussy
• Germany
  • Bavaria
    • Erlangen, Bavaria, Germany, 91054
      • Universitaetsklinikum Erlangen
  • DEU
    • Berlin, DEU, Germany, 13125
      • HELIOS Klinikum Berlin-Buch Saarow
    • Berlin, DEU, Germany, 13353
      • Charite - Universitaetsmedizin Berlin
    • Dresden, DEU, Germany, 1307
      • Universitaetsklinik Dresden
    • Essen, DEU, Germany, 45147
      • University Hospital Essen
    • Frankfurt Am Main, DEU, Germany, 60488
      • Institut fr Klinisch Onkologische ForschungKrankenhaus Nordwest GmbH
    • Hamburg, DEU, Germany, 20249
      • Haematologisch-Onkologische Praxis Hamburg Eppendorf
    • Hamburg, DEU, Germany, 22763
      • Asklepios Tumorzentrum Hamburg AK Altona
    • Leipzig, DEU, Germany, 4103
      • Universitaeres Krebszentrum Leipzig
    • Ludwigsburg, DEU, Germany, 22763
      • RKH Kliniken
    • Mannheim, DEU, Germany, 68167
      • Universitaetsmedizin Mannheim- III. Medizinische Klinik
    • Muenchen, DEU, Germany, 81737
      • Klinikum Neuperlach
    • Porta Westfalica, DEU, Germany, 32457
      • Zentrum für Hämatologie und Onkologie MVZ GmbH
• Hungary
  • Gyula, Hungary, 5700
    • Bekes Megyei Kozponti Korhaz, Pandy Kalman Tagkorhaz, Megyei Onkologiai Kozpont
  • HUN
    • Budapest, HUN, Hungary, 1097
      • Del-Pesti Centrumkorhaz Orszagos Hematologiai es Infektologiai Intezet, Szent Laszlo Korhaz
    • Budapest, HUN, Hungary, 1122
      • National Institute of Oncology
    • Budapest, HUN, Hungary, H-1062
      • Magyar Honvédség Egészségügyi Központ
    • Debrecen, HUN, Hungary, 4032
      • Debreceni Egyetem Klinikai Kozpont
    • Kecskemét, HUN, Hungary, 6000
      • Bacs- Kiskun Megyei Korhaz
    • Nyiregyhaza, HUN, Hungary, 4400
      • Szabolcs-Szatmar-Bereg Megyei Korhazak es Egyetemi Oktatokorhaz
    • Szolnok, HUN, Hungary, 5004
      • Hetenyi G Korhaz, Onkologiai Kozpont
    • Tatabanya, HUN, Hungary, 2800
      • Szent Borbala Korhaz
  • Somogy
    • Kaposvár, Somogy, Hungary, 7400
      • Somogy Megyei Kaposi Mor Oktato Korhaz, Klinikai Onkologiai Osztaly
  • Zala
    • Zalaegerszeg, Zala, Hungary, 8900
      • Zala Megyei Szent Rafael Korhaz, Onkologiai Osztaly, F epulet 3. em.
• Italy
  • ITA
    • Brescia, ITA, Italy, 25124
      • Fondazione Poliambulanza Hospital
    • Genova, ITA, Italy, 16132
      • Policlinico San Martino di Genova
    • Milano, ITA, Italy, 20133
      • Fondazione IRCCS Istituto Nazionale dei Tumori
    • Milano, ITA, Italy, 20162
      • ASST Grande Ospedale Metropolitano Niguarda
    • Naples, ITA, Italy, 80131
      • Istituto Nazionale Tumori IRCCS Fondazione G. Pascale
    • Padova, ITA, Italy, 35128
      • Istituto Oncologico Veneto IRCCS
    • Pisa, ITA, Italy, 56126
      • Azienda Ospedaliero Universitaria Pisana
    • Reggio Emilia, ITA, Italy, 42123
      • Azienda USL-IRCCS Di Reggio Emilia
    • Tricase, ITA, Italy, 73039
      • AO Card G Panico
    • Vicenza, ITA, Italy, 36100
      • Ospedale San Bortolo Azienda ULSS8 Berica - Distretto Est
  • Lombardy
    • Rozzano MI, Lombardy, Italy, 20089
      • Istituto Clinico Humanitas
• Japan
  • Aichi
    • Nagoya, Aichi, Japan, 464-8681
      • Aichi Cancer Center
  • Chiba
    • Kashiwa-shi, Chiba, Japan, 277-8577
      • National Cancer Center Hospital East
  • Ehime
    • Matsuyama City, Ehime, Japan, 791-0280
      • Shikoku Cancer Center
  • Fukuoka
    • Fukuoka-shi, Fukuoka, Japan, 811-1395
      • Kyushu Cancer Center
  • Hokkaido
    • Sapporo-shi, Hokkaido, Japan, 060-8648
      • Hokkaido University Hospital
  • Kanagawa
    • Kawasaki-shi, Kanagawa, Japan, 216-8511
      • St. Marianna University School of Medicine Hospital
  • Osaka
    • Osakasayama-shi, Osaka, Japan, 589-8511
      • Kindai University Hospital
    • Suita-shi, Osaka, Japan, 565-0871
      • Osaka University Hospital
  • Sunto-gun
    • Shizuoka, Sunto-gun, Japan, 411-8777
      • Shizuoka Cancer Center
  • Tokyo
    • Chuo-ku, Tokyo, Japan, 104-0045
      • National Cancer Center Hospital
• Poland
  • Masovia
    • Warszawa, Masovia, Poland, 02034
      • M Sklodowska Curie Memorial Cancer Center, Klinika Gastroenterologii Onkologicznej
  • Podlaskie
    • Bialystok, Podlaskie, Poland, 15-027
      • Bialostockie Centrum Onkologii im. Marii Skodowskiej-Curie
• Spain
  • Madrid, Spain, 28007
    • Hospital General Universitario Gregorio Maranon HGUGM
  • Sevilla, Spain, 41013
    • Hospital Universitario Virgen del Rocio
  • Valencia, Spain, 46010
    • Hospital Clínico Universitario de Valencia
  • ESP
    • Barcelona, ESP, Spain, 8035
      • Hospital Universitari Vall dHebron
    • Córdoba, ESP, Spain, 14004
      • Hospital Universitario Reina Sofa
    • Elche, ESP, Spain, 3203
      • Hospital General Universitario de Elche
    • Madrid, ESP, Spain, 28034
      • Hospital Universitario Ramón y Cajal
    • Madrid, ESP, Spain, 28040
      • Hospital Clinico San Carlos
    • Madrid, ESP, Spain, 28041
      • Hospital Universitario 12 de octubre
    • Madrid, ESP, Spain, 28046
      • Hospital Universitario La Paz
    • Madrid, ESP, Spain, 28050
      • Hospital Universitario HM Sanchinarro
    • Majadahonda, ESP, Spain, 28222
      • Hospital Universitario Puerta de Hierro
    • Malaga, ESP, Spain, 29010
      • Hospital Regional Universitario Carlos Haya
    • Oviedo, ESP, Spain, 33013
      • Hospital Universitario Central de Asturias
    • Santander, ESP, Spain, 39008
      • Hospital Universitario Marques de Valdecilla
    • Santiago De Compostela, ESP, Spain, 15706
      • Hospital ClÃ-nico Universitario de Santiago-CHUS
• United Kingdom
  • GBR
    • Aberdeen, GBR, United Kingdom, AB25 2ZN
      • Aberdeen Royal Infirmary
    • London, GBR, United Kingdom, SW3 6JJ
      • The Royal Marsden Hospital
  • Middlesex
    • London, Middlesex, United Kingdom, W1G 6AD
      • Sarah Cannon Research Institute UK
• United States
  • Arizona
    • Phoenix, Arizona, United States, 85054
      • Mayo Clinic Arizona
    • Tucson, Arizona, United States, 85704
      • Arizona Oncology Associates, PC-Hope
  • California
    • Los Angeles, California, United States, 90027
      • California Research Institute (CRI)
    • Los Angeles, California, United States, 91010
      • City of Hope Comprehensive Cancer Center
  • Colorado
    • Aurora, Colorado, United States, 80012
      • Rocky Mountain Cancer Center
  • District of Columbia
    • Washington, District of Columbia, United States, 20052
      • The George Washington University Medical Center
  • Florida
    • Fort Myers, Florida, United States, 33901
      • Sarah Cannon Research Institute-S-Ft. Myers (FCS South)
    • Jacksonville, Florida, United States, 32224
      • Mayo Clinic Florida
    • Miami Beach, Florida, United States, 33140
      • Mount Sinai Medical Center
    • Palm Bay, Florida, United States, 32901
      • Cancer Care Centers of Brevard, Inc.
    • Saint Petersburg, Florida, United States, 33705
      • Sarah Cannon Research Institute-N-St Pete (FCS North)
    • Tallahassee, Florida, United States, 32308
      • Sarah Cannon Research Institute-Pan-Tallahassee (FCS Panhandle)
    • West Palm Beach, Florida, United States, 33401
      • Sarah Cannon Research-E-WPB (Florida Cancer Specialists-FCS East)
  • Georgia
    • Atlanta, Georgia, United States, 30322
      • Emory Winship Cancer Institute
  • Illinois
    • Arlington Heights, Illinois, United States, 60005
      • Illinois Cancer Specialists
    • Chicago, Illinois, United States, 60637
      • University of Chicago Medical Center
    • Chicago Ridge, Illinois, United States, 60415
      • Affiliated Oncologists
  • Kansas
    • Garden City, Kansas, United States, 67846
      • XCancer / Central Care Cancer Center
  • Kentucky
    • Louisville, Kentucky, United States, 40202
      • University of Louisville - James Brown Cancer Center
    • Louisville, Kentucky, United States, 40217
      • Norton Cancer Institute Audubon
  • Louisiana
    • Baton Rouge, Louisiana, United States, 70809
      • Hematology Oncology Clinic
    • Hammond, Louisiana, United States, 70403
      • XCancer / Pontchartrain Cancer Center
  • Maryland
    • Columbia, Maryland, United States, 21044
      • Maryland Oncology Hematology, P.A.
  • Michigan
    • Ann Arbor, Michigan, United States, 48109
      • University of Michigan Health System
    • Detroit, Michigan, United States, 48201
      • Barbara Ann Karmanos Cancer Institute
  • Minnesota
    • Minneapolis, Minnesota, United States, 55404
      • Minnesota Oncology
    • Rochester, Minnesota, United States, 55905
      • Mayo Clinic Rochester
  • Missouri
    • Kansas City, Missouri, United States, 64114
      • Center for Pharmaceutical Research
  • Nevada
    • Las Vegas, Nevada, United States, 89169
      • Comprehensive Cancer Centers of Nevada
  • New Jersey
    • New Brunswick, New Jersey, United States, 08901
      • Rutgers Cancer Institute of New Jersey
  • New Mexico
    • Albuquerque, New Mexico, United States, 87109
      • XCancer / New Mexico Oncology & Hematology Consultants
  • South Carolina
    • Charleston, South Carolina, United States, 29414
      • Charleston Oncology
  • Tennessee
    • Nashville, Tennessee, United States, 37203
      • Sarah Cannon Tennessee Oncology
    • Nashville, Tennessee, United States, 37232
      • Vanderbilt Ingram Cancer Center
  • Texas
    • Austin, Texas, United States, 78705
      • Texas Oncology - Austin
    • Dallas, Texas, United States, 75246
      • Texas Oncology Baylor Sammons
    • El Paso, Texas, United States, 79902
      • Texas Oncology-El Paso
    • Houston, Texas, United States, 77030
      • MD Anderson Cancer Center
    • McAllen, Texas, United States, 78503
      • Texas Oncology-McAllen
    • San Antonio, Texas, United States, 78217
      • Texas Oncology-San Antonio
    • Tyler, Texas, United States, 75702
      • Texas Oncology-Tyler
  • Virginia
    • Norfolk, Virginia, United States, 23502
      • Virginia Oncology Associates
  • Washington
    • Everett, Washington, United States, 98201
      • Providence Regional Cancer Partnership
    • Vancouver, Washington, United States, 98684
      • Northwest Cancer Specialists, P.C.
  • Wisconsin
    • Milwaukee, Wisconsin, United States, 53226
      • Medical College of Wisconsin/ Froedtert Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Provide written informed consent;
• Age ≥18 years;
• Histologically and/or cytologically documented metastatic colorectal adenocarcinoma. RAS, BRAF, and microsatellite instability microsatellite instability (MSI)/mismatch repair (MMR) status for each patient must be documented, according to country level guidelines;
• Participants must have progressed on or been intolerant to treatment with either trifluridine/tipiracil (TAS-102) or regorafenib. Participants are considered intolerant to TAS-102 or regorafenib if they have received at least 1 dose of either agents and were discontinued from therapy for reasons other than disease progression. Participants who have been treated with both TAS-102 and regorafenib are permitted. Participants must also have been previously treated with standard approved therapies: fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy, an anti-VEGF biological therapy, and, if RAS wild-type, an anti-EGFR therapy;
• Participants with microsatellite-high (MSI-H) or mismatch repair deficient (dMMR) tumors must have been treated with immune checkpoint inhibitors if approved and available in the participant's country unless the patient is ineligible for treatment with a checkpoint inhibitor;
• Participants who received oxaliplatin in the adjuvant setting and developed metastatic disease during or within 6 months of completing adjuvant therapy are considered eligible without receiving oxaliplatin in the metastatic setting. Participants who developed metastatic disease more than 6 months after completion of oxaliplatin-containing adjuvant treatment must be treated with oxaliplatin-based therapy in the metastatic setting to be eligible;
• Body weight ≥40kg;
• Eastern Cooperative Oncology Group (ECOG) performance status of 0-1;
• Have measurable disease according to RECIST Version 1.1, assessed locally. Tumors that were treated with radiotherapy are not measurable per RECIST Version 1.1, unless there has been documented progression of those lesions;
• Expected survival >12 weeks.
• For female participants of childbearing potential and male participants with partners of childbearing potential, agreement to use a highly effective form(s) of contraception, that results in a low failure rate (<1% per year) when used consistently and correctly, starting during the screening period, continuing throughout the entire study period, and for 90 days after taking the last dose of study drug. Such methods include: oral hormonal contraception (combined estrogen/ progestogen, or progestogen-only) associated with inhibition of ovulation, intrauterine device (IUD), intrauterine hormone-releasing system (IUS), bilateral tubal ligation, vasectomized partner, or true sexual abstinence in line with the preferred and usual lifestyle of the participant. Highly effective contraception should always be combined with an additional barrier method (eg, diaphragm, with spermicide). The same criteria are applicable to male participants involved in this clinical trial if they have a partner of childbirth potential, and male participants must always use a condom.
• Participants with BRAF-mutant tumors must have been treated with a BRAF inhibitor if approved and available in the participant's home country unless the patient is ineligible for treatment with a BRAF inhibitor.

Exclusion Criteria:

• Absolute neutrophil count (ANC) <1.5×109/L, platelet count <100×109/L, or hemoglobin <9.0 g/dL. Blood transfusion within 1 week prior to enrollment for the purpose of increasing the likelihood of eligibility is not allowed;
• Serum total bilirubin >1.5 × the upper limit of normal (ULN). Participants with Gilbert syndrome, bilirubin <2 X ULN, and normal AST/ALT are eligible;
• Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) >2.5 × ULN in participants without hepatic metastases; ALT or AST >5 × ULN in participants with hepatic metastases;
• Serum creatinine >1.5 × ULN or creatinine clearance <60 mL/min. Creatinine clearance can either be measured in a 24-hour urine collection or estimated by the Cockroft-Gault equation.
• Urine dipstick protein ≥2+ or 24-hour urine protein ≥1.0 g/24-h. Participants with greater than 2+ proteinuria by dipstick must undergo a 24-hour urine collection to assess urine protein level;
• Uncontrolled hypertension, defined as: systolic blood pressure ≥140 mm Hg and/or diastolic blood pressure ≥90 mm Hg despite optimal medical management. Participants were required to have blood pressure values below both limits. Repeated assessments were permitted;
• International Normalized Ratio (INR) >1.5 x ULN or activated partial thromboplastin time (aPTT) >1.5 × ULN, unless the patient is currently receiving or intended to receive anticoagulants for prophylactic purposes;
• History of, or active gastric/duodenal ulcer or ulcerative colitis, active hemorrhage of an unresected gastrointestinal tumor, history of perforation or fistulas; or any other condition that could, in the investigator's judgment, result in gastrointestinal hemorrhage or perforation; within the 6 months prior to screening;
• History or presence of hemorrhage from any other site (eg, hemoptysis or hematemesis) within 2 months prior to screening;
• History of a thromboembolic event, including deep vein thrombosis (DVT), pulmonary embolism (PE), or arterial embolism within 6 months prior to screening.
• Stroke and/or transient ischemic attack within 12 months prior to screening;
• Clinically significant cardiovascular disease, including but not limited to acute myocardial infarction or coronary artery bypass surgery within 6 months prior to enrollment, severe or unstable angina pectoris, New York Heart Association Class III/IV congestive heart failure, ventricular arrhythmias requiring treatment, or left ventricular ejection fraction (LVEF) <50% by echocardiogram;
• Mean corrected QT interval using the Fridericia method (QTcF) >480 msec or any factors that increase the risk of QTc prolongation or risk of arrhythmic events such as hypokalemia, congenital long QT syndrome, family history of long QT syndrome, or unexplained sudden death under 40 years of age in a first-degree relative.
• Concomitant medications with a known risk of causing QT prolongation and/or Torsades de Pointes.
• Systemic anti-neoplastic therapies (except for those described in Exclusion 18) or any investigational therapy within 4 weeks prior to the first dose of study drug, including chemotherapy, radical radiotherapy, hormonotherapy, biotherapy and immunotherapy;
• Systemic small molecule targeted therapies (eg, tyrosine kinase inhibitors) within 5 half-lives or 4 weeks (whichever is shorter) prior to the first dose of study drug;
• Palliative radiotherapy for bone metastasis/lesion within 2 weeks prior to the initiation of study drug;
• Brachytherapy (i.e., implantation of radioactive seeds) within 60 days prior to the first dose of study drug.
• Use of strong inducers or inhibitors of CYP3A4 within 2 weeks (or 5 half-lives, whichever is longer) before the first dose of study drug;
• Surgery or invasive procedure (i.e., a procedure that includes a biopsy; central venous catheter placement is allowed) within 60 days prior to the first dose of study drug or unhealed surgical incision;
• Any unresolved toxicities from a previous antitumor treatment greater than CTCAE v5.0 Grade 1 (except for alopecia or neurotoxicity grade≤2);
• Known human immunodeficiency virus (HIV) infection;
• Known history of active viral hepatitis. For participants with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated. Participants with HCV infection who are currently on treatment are eligible if they have an undetectable HCV viral load.
• Clinically uncontrolled active infection requiring IV antibiotics;
• Tumor invasion of a large vascular structure, eg, pulmonary artery, superior or inferior vena cava;
• Women who are pregnant or lactating;
• Brain metastases and/or spinal cord compression untreated with surgery and/or radiotherapy, and without clinical imaging evidence of stable disease for 14 days or longer; participants requiring steroids within 4 weeks prior to start of study treatment are excluded;
• Other malignancy, except for non-melanoma skin cancer, in situ cervical ca or bladder ca (Tis and T1) that have been adequately treated during the 5 years prior to screening;
• Inability to take medication orally, dysphagia or an active gastric ulcer resulting from previous surgery (eg, gastric bypass) or a severe gastrointestinal disease, or any other condition that investigators believe may affect absorption of the investigational product;
• Other disease, metabolic disorder, physical examination anomaly, abnormal laboratory result, or any other condition (e.g., current alcohol or drug abuse) that investigators suspect may prohibit use of the investigational product, affect interpretation of study results, or put the patient at undue risk of harm based on the investigator's assessment;
• Known hypersensitivity to fruquintinib (or placebo) or any of its inactive ingredients including the azo dyes Tartrazine - FD&C Yellow 5 and Sunset yellow FCF - FD&C Yellow 6;
• Participants who have received prior fruquintinib;
• Live vaccine <28days before the first dose of study drug(s). Seasonal vaccines for influenza are generally inactivated vaccines and are allowed. Intranasal vaccines are live vaccines and are not allowed.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Quadruple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Fruquintinib Plus Best Supportive Care (BSC) Group; Participants will be orally administered Fruquintinib 5 mg in combination with BSC once daily for 3 weeks of continuous dosing followed by a 1-week break (with each cycle length of 28 days).	Drug: Fruquintinib; Oral VEGFR inhibitor; Other Names: HMPL-013
Placebo Comparator: Placebo Plus BSC Group; Participants will be orally administered Placebo 5 mg in combination with BSC once daily for 3 weeks of continuous dosing followed by a 1-week break (with each cycle length of 28 days).	Drug: Placebo; Placebo capsule

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Overall Survival (OS)	OS was defined as the time (months) from date of randomization to death from any cause. OS was calculated as (date of death or last known alive - date of randomization + 1)/30.4375. Participants without report of death at the time of analysis will be censored at the date last known alive.	From date of randomization to death from any cause (up to 22 months)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Progression Free Survival (PFS), as Assessed by the Investigator Using Response Evaluation Criteria In Solid Tumors (RECIST) v1.1	PFS was defined as the time (months) from randomization until the first radiographic documentation of objective progression as assessed by investigator using RECIST v1.1, or death from any cause, whichever comes first. More specifically, PFS was determined using all data until the last evaluable visit prior to or on the date of: (i) radiographic disease progression (PD) per RECIST v1.1; (ii) withdrawal of consent to obtain additional scans on study; or (iii) initiation of subsequent anticancer therapy other than the study drugs, whichever was earlier. PD was defined as: at least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study, including baseline; an absolute increase of at least 5 mm in the sum of diameters of target lesions; and the appearance of one or more new lesions.	From randomization until the first documentation of objective progression or death, whichever comes first (up to 22 months)
Objective Response Rate (ORR) Per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1)	ORR was defined as the percentage of participants who achieved a best overall response of confirmed complete response (CR) or partial response (PR), per RECIST v1.1, as determined by the investigator. PR: At least a 30 percent (%) decrease in the sum of diameters of target lesions, taking as reference the baseline sum of diameters. CR: Disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) must have reduction in short axis to less than (<)10 millimeters (mm).	From randomization until the first documentation of best overall response (up to 22 months)
Disease Control Rate (DCR) Per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1)	DCR was defined as percentage of participants achieving a best overall response of confirmed CR, PR, or stable disease (SD) (for at least 7 weeks) per RECIST v1.1, as determined by the investigator. PR: At least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum of diameters. CR: Disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) must have reduction in short axis to <10 mm. SD: Neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for progressive disease (PD), taking as reference the smallest sum on study. PD: At least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (nadir), including baseline.	From randomization until the first documentation of best overall response (up to 22 months)
Duration of Response (DOR) Per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1)	DOR was defined as the time (in months) from the first occurrence of PR or CR by RECIST Version 1.1, until the first date that progressive disease is documented by RECIST Version 1.1, or death, whichever comes first. Only those participants with confirmed responses of CR or PR were included in this analysis. DOR was calculated as (date of death or PD or last assessment - date of first occurrence of confirmed CR or PR + 1)/30.4375.	From first occurrence of PR or CR until the first documentation progression or death, whichever comes first (up to 22 months
Number of Participants With Treatment-emergent Adverse Events (TEAEs) and Serious TEAEs	An adverse event (AE) was any untoward medical occurrence in a clinical investigation participant administered a pharmaceutical product and that does not necessarily have a causal relationship with this treatment. An AE was considered a TEAE if the onset date was on or after the start of study treatment or if the onset date was missing, or if the AE had an onset date before the start of study treatment but worsened in severity after the study treatment until 37 days after the last dose of study treatment or a new treatment of anti-tumor therapy, whichever was earlier. After this period, treatment-related SAEs were also considered as TEAEs. AEs with an unknown/not reported onset date were also included.	From start of study drug administration up to 22 months
Observed Plasma Concentrations of Fruquintinib and Metabolite M11	Plasma samples were collected from the participants at the defined time points. Plasma concentrations were measured using a validated, specific, and sensitive liquid chromatography tandem mass spectrometry method. M11 is the active metabolite for the study drug.	Cycle 1 (Day 1 and 21): Pre-dose, 1, 2, 3 and 4 hours; Cycle 2 (Day 21): Predose and 2 hours, Cycle 3 (Day 1): Pre-dose, Cycle 3 (Day 21): Pre-dose and 2 hours, Cycle 5, 7, 9, 11, 13, 15 and 17 (Day 1): Pre-dose (Each cycle = 28 days)
Change From Baseline of Electrocardiogram (ECG) Results - QTcF Intervals Using Fridericia's Formula	QT Interval: Ventricular depolarization plus ventricular repolarization Normal Range: 400 to 460 milliseconds (msec). QTc: QT interval corrected based on the patient's heart rate. QTcF: An electrocardiographic finding in which the QT interval corrected for heart rate using Fridericia's formula. QTc = QT/∛(RR) RR = Respiration rate.	Baseline, Cycle 1 (Day 1 and 21): Pre-dose, 1, 2, 3 and 4 hours; Cycle 2 and 3 (Day 21): Pre-dose (Each cycle = 28 days)
Change From Baseline of ECG Results -QTcB Intervals Using Bazzett's Formula	QT Interval: Ventricular depolarization plus ventricular repolarization Normal Range: 400 to 460 msec. QTc: QT interval corrected based on the patient's heart rate. QTcB: An electrocardiographic finding in which the QT interval corrected for heart rate using Bazzett's formula.	Baseline, Cycle 1 (Day 1 and 21): Pre-dose, 1, 2, 3 and 4 hours; Cycle 2 and 3 (Day 21): Pre-dose (Each cycle = 28 days)
Correlation Between Fruquintinib Exposure-response With Efficacy (OS) and Safety (AEs) Endpoints	As pre-specified in Exposure-Response final analysis report, fruquintinib exposures response with efficacy and safety endpoints were performed along with data from other clinical studies and the integrated analyses were to be reported separately. Data is not reported for this outcome measure as its analysis is still ongoing and will be reported after study completion.	Up to 42 months
Change From Baseline in European Organization for Research and Treatment of Cancer Quality of Life (QOL) Questionnaire Core 30 (EORTC QLQ-C30) Global Health Status/Quality of Life Scale Score	EORTC QLQ-C30 contains 30 items across 5 functional scales (physical, role, cognitive, emotional, and social), 9 symptom scales (fatigue, nausea and vomiting, pain, dyspnea, sleep disturbance, appetite loss, constipation, diarrhea, and financial difficulties) and global health status/QOL scale. EORTC QLQ-C30 contains 28 questions (4-point scale where 1=Not at all [best] to 4=Very Much [worst]) and 2 questions (7-point scale where 1=Very poor [worst] to 7= Excellent [best]). Raw scores are standardized and converted into scale scores ranging from 0 to 100. For global health status/QOL scale, higher scores represent better QOL. A negative change from baseline value indicates patient condition became worst. Change from baseline in the EORTC QLQ-C30 Global Health Status/Quality of Life Scale scores was performed by visit (i.e., cycle), using a restricted maximum likelihood (REML)-based mixed model repeated measures (MMRM) approach.	Baseline, Cycle 2, 3 and 4 (Each cycle=28 days)
Change From Baseline in EuroQoL 5 Dimension 5 Level (EQ-5D-5L) Visual Analog Scale (VAS) Score	The EQ-5D-5L is a self-reported health status questionnaire that consisted of six questions used to calculate a health utility score. There were two components to the EQ-5D-5L: a five-item health state profile that assessed mobility, self-care, usual activities, pain/discomfort, and anxiety/depression used to obtain an Index Utility Score and a general VAS score for health status. EQ-5D VAS was used to record participant's rating for his/her current health-related quality of life state on a vertical VAS with scores ranging from 0 to 100, where 0 = worst imaginable health state and 100 = best imaginable health state. The higher the score the better the health status. A negative change from baseline value represents patient condition became worse. Change from baseline in the EQ-5D-5L VAS scores was performed by visit (i.e. cycle), using a REML-based MMRM approach.	Baseline, Cycle 2, 3 and 4 (Each cycle=28 days)
Change From Baseline in EuroQoL 5 Dimension 5 Level (EQ-5D-5L) Health Utility Index Scores	EQ-5D-5L consisted of 2 components: health state profile and optional VAS. EQ-5D health state profile had 5 dimensions: mobility, self-care, usual activities, pain/discomfort, anxiety/depression. Each dimension has 5 levels: 1= no problem, 2= slight problem, 3= moderate problem, 4= severe problem, and 5= extreme problem. The response levels collected from the EQ-5D-5L five dimensions as a health profile are converted into an EQ-5D-5L index (utility) scores to represent participants' utility value. The range of health utility index score is from -0.285 to 1, where higher value indicates perfect health and a negative value represents a state worse than dead. Change from baseline in EQ-5D-5L health utility index scores was performed by visit (i.e., cycle), using a REML-based MMRM approach.	Baseline, Cycle 2, 3 and 4 (Each cycle=28 days)
Health Care Resource Utilization: Duration of Hospital Visits by Participants	Duration of hospital visit was calculated as = stop date - start date + 1. Mean and standard deviation data for duration of hospital visits (in days) by participants was reported in this outcome measure.	From start of study drug administration up to 22 months
Health Care Resource Utilization: Number of Participants With Any Concomitant Medications Prescribed	Number of participants with any concomitant medications prescribed were reported.	From start of study drug administration up to 22 months

Collaborators and Investigators

• Sponsor: Hutchison Medipharma Limited
• Investigators: Study Director: William Schelman, MD, PhD, HUTCHMED International Corporation

Publications and helpful links

General Publications

• Dasari A, Sobrero A, Yao J, Yoshino T, Schelman W, Yang Z, Chien C, Kania M, Tabernero J, Eng C. FRESCO-2: a global Phase III study investigating the efficacy and safety of fruquintinib in metastatic colorectal cancer. Future Oncol. 2021 Aug;17(24):3151-3162. doi: 10.2217/fon-2021-0202. Epub 2021 May 17.

Study record dates

Study Major Dates

• Study Start (Actual): August 12, 2020
• Primary Completion (Actual): July 29, 2022
• Study Completion (Estimated): March 1, 2024

Study Registration Dates

• First Submitted: March 24, 2020
• First Submitted That Met QC Criteria: March 25, 2020
• First Posted (Actual): March 26, 2020

Study Record Updates

• Last Update Posted (Actual): September 14, 2023
• Last Update Submitted That Met QC Criteria: September 8, 2023
• Last Verified: September 1, 2023

More Information

Terms related to this study

• Keywords: VEGF; colorectal; colon; mcrc; crc; metastatic colon; metastatic colorectal; VEGFR
• Additional Relevant MeSH Terms: Digestive System Diseases; Neoplasms; Neoplasms by Site; Gastrointestinal Neoplasms; Digestive System Neoplasms; Gastrointestinal Diseases; Colonic Diseases; Intestinal Diseases; Intestinal Neoplasms; Rectal Diseases; Colorectal Neoplasms
• Other Study ID Numbers: 2019-013-GLOB1

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No