NCT04974398

Brief Summary

This study is a randomized, double-blind, multi-center phase III clinical study to compare the efficacy and safety of penpulimab combined with chemotherapy and placebo combined with chemotherapy in the first-line treatment of recurrent or metastatic nasopharyngeal carcinoma.

Trial Health

82
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
296

participants targeted

Target at P50-P75 for phase_3

Timeline
7mo left

Started Aug 2021

Longer than P75 for phase_3

Geographic Reach
5 countries

56 active sites

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress88%
Aug 2021Dec 2026

First Submitted

Initial submission to the registry

July 13, 2021

Completed
10 days until next milestone

First Posted

Study publicly available on registry

July 23, 2021

Completed
24 days until next milestone

Study Start

First participant enrolled

August 16, 2021

Completed
4.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 23, 2026

Completed
10 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 23, 2026

Expected
Last Updated

April 13, 2025

Status Verified

April 1, 2025

Enrollment Period

4.5 years

First QC Date

July 13, 2021

Last Update Submit

April 10, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Progression-free survival (PFS)

    PFS assessed by BIRC based on RECIST v1.1 .

    Up to 2 years

Secondary Outcomes (9)

  • Overall survival(OS)

    Up to 4 years

  • Objective response rate (ORR)

    Up to 2 years

  • Duration of response (DoR)

    Up to 2 years

  • Disease control rate (DCR)

    Up to 2 years

  • Adverse event (AE)

    From the time of informed consent signed through 90 days after the last dose of penpulimab

  • +4 more secondary outcomes

Study Arms (2)

Group A

EXPERIMENTAL

Group A (study group): Penpulimab plus cisplatin/carboplatin and gemcitabine

Drug: Penpulimab

Group B

PLACEBO COMPARATOR

Group B (control group): Placebo plus cisplatin/carboplatin and gemcitabine

Drug: placebo

Interventions

Arm A: Penpulimab (200 mg, administered on Day 1 of each cycle, Q3W) +cisplatin (80 mg/m2) or carboplatin (AUC 5) (administered on Day 1 of each cycle, Q3W, up to 6 cycles) + gemcitabine (1000 mg/ m2, administered on Days 1 and 8 of each cycle, Q3W, up to 6 cycles), 3 weeks (21 days) per cycle; followed by penpulimab (200 mg, administered on Day 1 of each cycle, Q3W) as maintenance treatment.

Also known as: cisplatin/carboplatin, gemcitabine
Group A

Arm B: Placebo (200 mg, administered on Day 1 of each cycle, Q3W) + cisplatin (80 mg/m2) or carboplatin (AUC 5) (administered on Day 1 of each cycle, Q3W, up to 6 cycles) + gemcitabine (1000 mg/m2, administered on Days 1 and 8 of each cycle, Q3W, up to 6 cycles), every 3 weeks (21 days) per cycle; followed by placebo(200 mg, administered on Day 1 of each cycle, Q3W) as maintenance treatment. Subjects in Arm B will have the opportunity to crossover to openlabel treatment with penpulimab monotherapy after radiographic disease progression.

Also known as: cisplatin/carboplatin, gemcitabine
Group B

Eligibility Criteria

Age12 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Voluntarily signed written Informed Consent Form(ICF).
  • Main study: Age of ≥ 18 years and ≤ 75 years at the time of enrollment.
  • Substudy: Age of ≥ 12 years and \< 18 years. Weight≥ 35KG.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  • Expected survival of ≥ 3 months.
  • Histologically or cytologically confirmed nasopharyngeal carcinoma.
  • Subjects with primary metastatic (nasopharyngeal carcinoma, stage IVB defined by the Union for International Cancer Control and the American Joint Committee on Cancer Staging System edition 8) nasopharyngeal carcinoma who are not suitable for local treatment or radical treatment; subjects who have a local-regional recurrence and/or distant metastasis more than 6 months after the completion of prior radical treatment (radiotherapy with induction, concurrent, adjuvant chemotherapy)ï¼› No systemic treatment has been received for recurrent or metastatic diseases, not amendable to local treatment or have received local treatment for the local-regional recurrent disease
  • At least one measurable lesion according to RECIST v1.1;
  • Has adequate organ function.
  • All female and male subjects of reproductive potential must agree to use an effective method of contraception, as determined by the Investigator, during and for 150 days after the last dose of study treatment.

You may not qualify if:

  • Subjects with pathologically diagnosed nasopharyngeal adenocarcinoma or sarcoma.
  • Subjects have had another malignancy within 3 years before the first dose, except nasopharyngeal carcinoma. Subjects with other malignancies that have been cured by local therapy such as basal or cutaneous squamous cell carcinoma, superficial bladder cancer, cervix or breast carcinoma in situ are not excluded.
  • Participation in treatment with an investigational drug or use of an investigational device within 4 weeks before first study dosing.
  • Have previously received immunotherapy, including immune checkpoint inhibitors, immune checkpoint agonists , immune cell therapy, and other treatments against tumor immune mechanism.
  • Active autoimmune disease requiring systemic treatment within 2 years prior to initial administration, or as an autoimmune disease that can recur or for which treatment is planned determined by the investigator.
  • Active or past history of definite inflammatory bowel disease (e.g., Crohn's disease or ulcerative colitis).
  • History of immunodeficiency; those who test positive for HIV antibody; current chronic use of systemic corticosteroids or immunosuppressive agents.
  • Known history of allotransplantation and allogeneic hematopoietic stem cell transplantation.
  • Has known active Hepatitis B or Hepatitis C.
  • Active or untreated CNS metastases.
  • Subjects with peripheral neuropathy.
  • Unresolved toxicity from prior anti-tumor therapy, defined as toxicity that has not recovered .
  • Received a live vaccine within 30 days before the first dose or planned to receive a live vaccine during the study.
  • Known allergy to any study drug component; known history of serious hypersensitivity to other monoclonal antibodies.
  • Pregnant or nursing (lactating) women.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (56)

City of Hope

Duarte, California, 91010, United States

Location

Winship Cancer Institute/Emory University

Atlanta, Georgia, 30388, United States

Location

University of Michigan

Ann Arbor, Michigan, 48109, United States

Location

Icahn School of Medicine at Mount Sinai

New York, New York, 10029, United States

Location

Memorial Sloan Kettering Cancer Center

New York, New York, 10065, United States

Location

Chris O'Brien Lifehouse

Camperdown, New South Wales, Australia

Location

St Vincent's Public Hospital Sydney

Darlinghurst, New South Wales, 2010, Australia

Location

Genesis Care North Shore

St Leonards, New South Wales, 2065, Australia

Location

Sir Charles Gardner

Heidelberg, Victoria, 3084, Australia

Location

Austin Health

Nedlands, Western Australia, 6009, Australia

Location

Hospital de CĂ¢ncer de Barretos - FundaĂ§Ă£o Pio XII

Barretos, REG1, 14784-400, Brazil

Location

Grupo OncoclĂ­nicas

Botafogo, REG1, 22250-905, Brazil

Location

Hospital Bruno Born

Lajeado, REG1, 95900-000, Brazil

Location

Hospital Nossa Senhora da Conceicao

Porto Alegre, REG1, 91350-200, Brazil

Location

Centro de Estudos e Pesquisa de Hematologia

Santo André, REG1, 09060-650, Brazil

Location

Instituto do CĂ¢ncer do Estado de SĂ£o Paulo (ICESP)

SĂ£o Paulo, REG1, 01246-000, Brazil

Location

Centro de CĂ¢ncer A. C. Camargo

SĂ£o Paulo, REG1, 01509-900, Brazil

Location

Alberta Health Services (Tom Baker Cancer Centre)

Calgary, Alberta, T2N 4N2, Canada

Location

Toronto Sunnybrook Hospital

Toronto, Ontario, M4N 3M5, Canada

Location

The First Affiliated Hospital of Anhui Medical University

Hefei, Anhui, 230022, China

Location

Fujian Cancer Hospital

Fuzhou, Fujian, 350014, China

Location

The First Affiliated Hospital of Xiamen University

Xiamen, Fujian, 361003, China

Location

Dongguan People's Hospital

Dongguan, Guangdong, 523058, China

Location

The First Affiliated Hospital of Sun Yat-sen University

Guangzhou, Guangdong, 510080, China

Location

Affiliated Cancer Hospital and Institute of Guangzhou Medical University

Guangzhou, Guangdong, 510095, China

Location

Sun Yat-sen Memorial Hospital, Sun Yat-sen University

Guangzhou, Guangdong, 510120, China

Location

The First Affiliated Hospital of Guangzhou Medical University

Guangzhou, Guangdong, 510120, China

Location

Zhujiang Hospital of Southern Medical University

Guangzhou, Guangdong, 510260, China

Location

Nanfang Hospital, Southern Medical University

Guangzhou, Guangdong, 510515, China

Location

The Sixth Affiliated Hospital of Sun Yat-sen University

Guangzhou, Guangdong, 510655, China

Location

The First Affiliated Hospital of Guangdong Pharmaceutical University

Guangzhou, Guangdong, 510699, China

Location

Guangzhou Panyu Central Hospital

Guangzhou, Guangdong, 511400, China

Location

Jiangmen Central Hospital

Jiangmen, Guangdong, 529000, China

Location

Cancer Hospital of Shantou University Medical College

Shantou, Guangdong, 515041, China

Location

Shenzhen People's Hospital

Shenzhen, Guangdong, 518020, China

Location

Affiliated Hospital of Guangdong Medical University

Zhanjiang, Guangdong, 524000, China

Location

The Fifth Affiliated Hospital of Sun Yat-sen University

Zhuhai, Guangdong, 519000, China

Location

Affiliated Hospital of Guilin Medical University

Guilin, Guangxi, 541001, China

Location

The People's Hospital of Guangxi Zhuang Autonomous Region

Nanning, Guangxi, 530016, China

Location

Guangxi Medical University Cancer Hospital

Nanning, Guangxi, 530021, China

Location

The First Affiliated Hospital of Guangxi Medical University

Nanning, Guangxi, 530021, China

Location

Guizhou Cancer Hospital

Guiyang, Guizhou, 550000, China

Location

The First Affiliated Hospital of Hainan Medical University

Haikou, Hainan, 570102, China

Location

Hainan General Hospital

Haikou, Hainan, 570311, China

Location

Hubei Cancer Hospital

Wuhan, Hubei, 430079, China

Location

The Second Xiangya Hospital of Central South University

Changsha, Hunan, 410012, China

Location

Hunan Cancer Hospital

Changsha, Hunan, 410031, China

Location

The First Affiliated Hospital of University of South China

Hengyang, Hunan, 421001, China

Location

The Second Affiliated Hospital of Nanchang University

Nanchang, Jiangxi, 330002, China

Location

Jiangxi Cancer Hospital

Nanchang, Jiangxi, 330029, China

Location

Fudan University Shanghai Cancer Center

Shanghai, Shanghai Municipality, 200032, China

Location

Sichuan Cancer Hospital

Chengdu, Sichuan, 610042, China

Location

The Affiliated Hospital of Southwest Medical University

Luzhou, Sichuan, 646000, China

Location

Yunnan Cancer Hospital

Kunming, Yunnan, 650118, China

Location

Zhejiang Cancer Hospital

Hangzhou, Zhejiang, 310005, China

Location

Taizhou Hospital of Zhejiang Province

Taizhou, Zhejiang, 317099, China

Location

MeSH Terms

Conditions

Nasopharyngeal Carcinoma

Interventions

penpulimabCisplatinCarboplatinGemcitabine

Condition Hierarchy (Ancestors)

CarcinomaNeoplasms, Glandular and EpithelialNeoplasms by Histologic TypeNeoplasmsNasopharyngeal NeoplasmsPharyngeal NeoplasmsOtorhinolaryngologic NeoplasmsHead and Neck NeoplasmsNeoplasms by SiteNasopharyngeal DiseasesPharyngeal DiseasesStomatognathic DiseasesOtorhinolaryngologic Diseases

Intervention Hierarchy (Ancestors)

Chlorine CompoundsInorganic ChemicalsNitrogen CompoundsPlatinum CompoundsCoordination ComplexesOrganic ChemicalsHeterocyclic CompoundsDeoxycytidineCytidinePyrimidine NucleosidesPyrimidinesHeterocyclic Compounds, 1-Ring

Study Officials

  • Chaosu Hu, MD

    Fudan University

    PRINCIPAL INVESTIGATOR
  • Xiaozhong Chen, MD

    Cancer Hospital of The University of Chinese Academy of Sciences

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 3
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 13, 2021

First Posted

July 23, 2021

Study Start

August 16, 2021

Primary Completion

February 23, 2026

Study Completion (Estimated)

December 23, 2026

Last Updated

April 13, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will share

Individual anonymized participant data will be considered for sharing once the product and indication have been approved by major health authorities, if there is legal authority to share the data and there is no reasonable likelihood of participant reidentification. Data may be requested from the corresponding author.

Shared Documents
STUDY PROTOCOL, SAP
Time Frame
The study protocol and SAP will be available when the main results of this study are officially published in a scientific journal.
Access Criteria
The study protocol and SAP can be obtained by emailing to the corresponding author of the published paper.

Locations