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AzTrials

Non-Small Cell Lung CancerPhase 3DUBLIN-3NCT02504489

Docetaxel + Plinabulin Compared to Docetaxel + Placebo in Patients With Advanced NSCLC

A Phase 3 study testing Docetaxel + Plinabulin (DP) and Docetaxel (D) in people with Non-Small Cell Lung Cancer, run by BeyondSpring Pharmaceuticals Inc. at 57 sites in 3 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

To compare the overall survival of NSCLC patients receiving 2nd- or 3rd-line systemic therapy with docetaxel + plinabulin (DP Arm) to patients treated with docetaxel + placebo (D5W) (D Arm) for advanced or metastatic disease. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Non-Small Cell Lung Cancer
What is being tested?
Docetaxel + Plinabulin (DP) and Docetaxel (D)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
559 participants
Where
57 sitesin 3 countries
Study dates
Dec 2015to 30 Oct 2023
Phase
Phase 3
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Males and females ≥ 18 years of age
  • ECOG performance status ≤ 2.
  • Histopathologically or cytologically confirmed non-squamous or squamous NSCLC.
  • Disease progression during or after treatment with one or two treatment regimen(s) Treatment regimens can be chemotherapy, targeted therapy, biological therapy, or immunotherapy for advanced (Stage IIIB) or metastatic disease (Stage IV). Modification of a regimen to manage toxicity with a different drug does not constitute a new regimen. Maintenance therapy following platinum-based chemotherapy is not considered as a separate regimen. Adjuvant or neoadjuvant chemotherapy and/or chemo-radiation for early stage disease do not count as prior systemic therapy. Prior radiation therapy is not exclusionary. Prior immunotherapy with a PD-1/PD-L1 inhibitor is not exclusionary. Prior treatment for advanced or metastatic disease must have included a platinum-based regimen. (Treatment of early stage disease [Stage IIIA or earlier] with a platinum-containing therapy does not count).
  • Patients with active brain metastasis or leptomeningeal involvement with brain metastases who are asymptomatic, and whose lesions by imaging are at least stable and without interim development of new lesions for at least 4 weeks may be enrolled. Patients who require continued therapy with steroid medication for management for their brain metastases are eligible; dosing must be stable for at least 4 weeks prior to randomization;
  • Patients must have at least one measurable lung lesion of ≥10 mm by CT or MRI per RECIST 1.1 criteria. Radiographic tumor assessment is to be performed within 28 days prior to randomization;
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  • All patients with non-squamous NSCLC must have been tested for 19 deletion and exon 21 L858R substitution mutation. Only patients without EGFR sensitizing mutations are eligible, and they must have progressed on platinum-based chemotherapy. Patients with known ALK-rearrangements should be treated with an appropriate tyrosine kinase inhibitor (TKI) before entering the study. The TKI regimen would count as a line of treatment.
  • All adverse events of any prior systemic therapy, surgery, or radiotherapy, must have resolved to CTCAE (v4.03) Grade ≤2, except for neurological adverse events that must have resolved to Grade ≤1;
  • The following laboratory results from the central laboratory within 14 days prior to Cycle 1 Day 1 study drug administration.
  • Hemoglobin ≥9 g/dL independent of transfusion or growth factor support;
  • Absolute neutrophil count ≥1.5 x 109/L independent of growth factor support;
  • Platelet count ≥100 x 109/L independent of transfusion or growth factor support;
  • Serum total bilirubin ≤ ULN, unless the patient has a diagnosis of Gilbert's disease in which case serum bilirubin ≤3.0 times ULN;
  • AST and ALT ≤2.5 x ULN (≤1.5 x ULN if alkaline phosphatase is >2.5 x ULN);
  • Serum creatinine ≤1.5 x ULN;
  • Life expectancy more than 12 weeks;
  • Female patients of childbearing potential have a negative pregnancy test at baseline. Females of childbearing potential are defined as sexually mature women without prior hysterectomy or who have had any evidence of menses in the past 12 months. However, women who have been amenorrheic for 12 or more months are still considered to be of childbearing potential if the amenorrhea is possibly due to prior chemotherapy, anti-estrogens, or ovarian suppression.
  • Women of childbearing potential (i.e., menstruating women) must have a negative urine pregnancy test (positive urine tests are to be confirmed by serum test) documented within the 24-hour period prior to the first dose of study drug.
  • Sexually active women of childbearing potential enrolled in the study must agree to use two forms of accepted methods of contraception during the course of the study and for 3 months after their last dose of study drug. Effective birth control includes (a) intrauterine device (IUD) plus one barrier method; (b) on stable doses of hormonal contraception for at least 3 months (e.g., oral, injectable, implant, transdermal) plus one barrier method; (c) 2 barrier methods. Effective barrier methods are male or female condoms, diaphragms, and spermicides (creams or gels that contain a chemical to kill sperm); or (d) a vasectomized partner.
  • For male patients who are sexually active and who are partners of premenopausal women: agreement to use two forms of contraception as in criterion 11b above during the treatment period and for at least 3 months after the last dose of study drug.
  • Signed informed consent.

Who cannot join

  • Administration of chemotherapy, immunotherapy, biological, targeted, or radiation therapy or investigational agent (therapeutic or diagnostic) within 3 weeks prior to receipt of study medication. Major surgery, other than diagnostic surgery, within 4 weeks before first study drug administration.
  • Significant cardiac history:
  • History of myocardial infarction or ischemic heart disease within 1 year (within a window of 18 days) before first study drug administration;
  • Uncontrolled arrhythmia;
  • History of congenital QT prolongation;
  • ECG findings consistent with active ischemic heart disease;
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  • New York Heart Association Class III or IV cardiac disease;
  • Uncontrolled hypertension: blood pressure consistently greater than 150 mm Hg systolic and 100 mm Hg diastolic in spite of antihypertensive medication.
  • Patients who have received prior treatment with docetaxel.
  • Prior transient ischemic attack or cerebrovascular accident within the past year (within an 18-day window). Any neurologic toxicities ≥ Grade 2 within 3 weeks of randomization.
  • History of hemorrhagic diarrhea, inflammatory bowel disease or active uncontrolled peptic ulcer disease. (Concomitant therapy with ranitidine or its equivalent and/or omeprazole or its equivalent is acceptable). History of ileus or other significant gastrointestinal disorder known to predispose to ileus or chronic bowel hypomotility.
  • Active uncontrolled bacterial, viral, or fungal infection requiring systemic therapy.
  • Known infection with human immunodeficiency virus (HIV) or active hepatitis A, B, or C.
  • Known prior hypersensitivity reaction to any product containing polysorbate 80, polyoxyethylene 15 hydroxystearate/Macrogol 15 hydroxystearate (Solutol HS 15/ Kolliphor HS 15).
  • Female subject who is pregnant or lactating.
  • Second malignancy unless in remission for >5 years. (Non-melanoma skin cancer or carcinoma in situ of the cervix treated with curative intent is not exclusionary).
  • Any medical conditions that, in the Investigator's opinion, would impose excessive risk to the patient. Examples of such conditions include uncontrolled diabetes, infection requiring parenteral anti-infective treatment, liver failure, any altered mental status or any psychiatric condition that would interfere with the understanding of the informed consent form.
  • Unwilling or unable to comply with procedures required in this protocol.

Trial locations and contacts

57 sites in 3 countries.

57 sites in 3 countries

China29 sites
  • Cancer Hospital Chinese Academy of Medical Science

    Beijing, Beijing Municipality, 100021

  • Beijing Cancer Hospital

    Beijing, Beijing Municipality, 100142

  • The PLA General Hospital

    Beijing, Beijing Municipality, 100853

  • Jilin Province Cancer Hospital

    Changchun, Jilin, 100013

  • The Second Xiangya Hospital of Central South Unive

    Changsha, Hunan, 410011

  • West China Hospital of Sichuan University

    Chengdu, Sichuan, 610041

  • Guizhou Provincial Hospital

    Guiyang, Guizhou, 550002

  • Sir Run Run Shaw Hospital, Zhejiang University

    Hangzhou, Zhejiang, 310016

  • Zhejiang Cancer Hospital

    Hangzhou, Zhejiang, 310022

  • The First Affiliated Hospital, Zhejiang University

    Hanzhou, Zhejiang, 310003

  • Affiliated Cancer Hospital of Harbin Medical Unive

    Harbin, Heilongjiang, 150040

  • Anhui Provincial Hospital

    Hefei, Anhui, 230000

  • Jiangyin People's Hospital

    Jiangyin, Jiangsu, 214400

  • Shandong Cancer Hospital

    Jinan, Shangdong, 250117

  • 527-Linyi Cancer Hospital

    Linyi, Shangdong, 276000

  • Jiangxi Provincial Tumor Hospital

    Nanchang, Jiangxi, 330000

  • Jiangsu Cancer Hospital

    Nanjing, Jiangsu, 210009

  • Nantong Tumor Hospital

    Nantong, Jiangsu, 226361

  • Shanghai Chest Hospital, Shanghai Jiaotong Univers

    Shanghai, Shanghai Municipality, 200030

  • The Fifth People's Hospital of Shanghai

    Shanghai, Shanghai Municipality, 200240

  • Liaoning Cancer Hospital & Institute

    Shenyang, Liaoning, 110042

  • The Fourth Hospital of Hebei Medical University

    Shijiazhuang, Hebei, 050011

  • Tianjin People's Hospital

    Tianjin, Tianjin Municipality, 300060

  • Affiliated Tumor Hospital of Xinjiang Medical Univ

    Ürümqi, Xinjiang, 830011

  • The First Affiliated Hospital of Xi'an Jiaotong U

    Xi'an, Shaanxi, 710061

  • The First Affiliated Hospital of Xiamen University

    Xiamen, Fujian, 361000

  • Zhongshan Hospital Xiamen University

    Xiamen, Fujian, 361000

  • Yantai Yuhuangding Hospital

    Yantai, Shangdong, 264000

  • Henan Cancer Hospital

    Zhengzhou, Henan, 450008

Other trials in China

United States19 sites
  • Pacific Cancer Medical Center, Inc.

    Anaheim, California, 92801

  • Peachtree Hematoloy-Oncology Consultants, PC

    Atlanta, Georgia, 30318

  • Central Care Cancer Center

    Bolivar, Missouri, 65613

  • Ironwood Cancer & Research Centers

    Chandler, Arizona, 85224

  • University of Cincinnati

    Cincinnati, Ohio, 45267

  • Memorial Health Care System

    Colorado Springs, Colorado, 80909

  • Cookeville Regional Medical Center Cancer Center

    Cookeville, Tennessee, 61801

  • Henry Ford Hospital

    Detroit, Michigan, 48202

  • Michigan Center of Medical Research

    Farmington Hills, Michigan, 48334

  • Hattiesburg Clinic Hematology/Oncology

    Hattiesburg, Mississippi, 39401

  • University of Louisville-Brown Cancer Center

    Louisville, Kentucky, 40202

  • Allegheny Health Network

    Pittsburgh, Pennsylvania, 15212

  • Cancer Center of Central Connecticut

    Plainville, Connecticut, 06062

  • Orchard Healthcare Research Inc.

    Skokie, Illinois, 60077

  • Toledo Cancer Center

    Toledo, Ohio, 43623

  • Carle Cancer Center

    Urbana, Illinois, 61801

  • Kansas University Medical Center

    Westwood, Kansas, 00913

  • Innovative Clinical Research Institute

    Whittier, California, 90603

  • Wake Forest Baptist Health

    Winston-Salem, North Carolina, 27157

Other trials in United States

Australia9 sites
  • Blacktown Cancer Centre

    Blacktown, New South Wales, 2148

  • Border Medical Oncology Research Unit

    East Albury, New South Wales, 2640

  • Gosford Hospital

    Gosford, New South Wales, 2250

  • Peninsula and South East Oncology

    Melbourne, Victoria, 3199

  • Fiona Stanley Hospital

    Murdoch, Western Australia, 6150

  • Perth Oncology/Mount Hospital

    Perth, Western Australia, 6000

  • Epworth Hospital

    Richmond, Victoria, 3121

  • Adult Mater Hospital

    South Brisbane, Queensland, 4101

  • St John of God Hospital, Subiaco

    Subiaco, Western Australia, 6008

Other trials in Australia

About this study

Official title: Randomized Blinded Phase III Assessment of Second or Third-Line Chemotherapy With Docetaxel + Plinabulin Compared to Docetaxel + Placebo in Patients With Advanced Non-Small Cell Lung Cancer and With at Least One Measurable Lung Lesion

To compare the overall survival of NSCLC patients receiving 2nd- or 3rd-line systemic therapy with docetaxel + plinabulin (DP Arm) to patients treated with docetaxel + placebo (D5W) (D Arm) for advanced or metastatic disease.

Secondary purposes of the study are:

  • To compare overall response rate (ORR) of NSCLC patients receiving 2nd- or 3rd-line systemic therapy with docetaxel + plinabulin (DP Arm) to patients treated with docetaxel + placebo (D5W) (D Arm) for advanced or metastatic disease.
  • To compare progression free survival (PFS) of NSCLC patients receiving 2nd- or 3rd-line systemic therapy with docetaxel + plinabulin (DP Arm) to patients treated with docetaxel + placebo (D5W) (D Arm) for advanced or metastatic disease.
  • To compare incidence of Grade 4 neutropenia (absolute neutrophil count [ANC] < 0.5 × 109/L) on Day 8 (+/- 1 day) of Cycle 1 of NSCLC patients receiving 2nd- or 3rd-line systemic therapy with docetaxel + plinabulin (DP Arm) to patients treated with docetaxel + placebo (D5W) (D Arm) for advanced or metastatic disease.
  • To compare 24-month and 36-month OS rate of NSCLC patients receiving 2nd- or 3rd-line systemic therapy with docetaxel + plinabulin (DP Arm) to patients treated with docetaxel + placebo (D5W) (D Arm) for advanced or metastatic disease.
Read the detailed description

Lung cancer is the leading cause of cancer-related mortality worldwide. According to the World Health Organization's Global Cancer Observatory, there were an estimated 2.09 million new cases and 1.76 million deaths worldwide in 2018 (GLOBOCAN, 2018, Fact Sheet N⁰39). The lung cancer incidence and mortality in China is relatively high compared to most countries with an estimated 774,323 new cases and 690,567 deaths in 2018 (GLOBOCAN, 2018, Fact Sheet N⁰160 China). In the US, as per the estimates of the National Cancer Institute, there would be about 228,820 new cases and 135,720 deaths from lung cancer in 2020 accounting for approximately 22.4% of all cancer deaths (SEER program, 2020). About 84% of lung cancers are NSCLCs in the US (American Cancer Society, 2020).

The prognosis for patients with advanced or metastatic NSCLC, either at initial diagnosis or recurrence, remains grim. The standard of care has been chemotherapy with agents including platinum analogs, taxanes, vinca alkaloids, and pemetrexed with vascular endothelial growth factor inhibitors and for patients with appropriate disease genotypes, epidermal growth factor receptor (EGFR) inhibitors or anaplastic lymphoma kinase (ALK) inhibitors.

First-line Therapy: For patients without specific molecular target, first-line therapy is usually a programmed cell death protein 1 (PD-1)-inhibitor or a platinum-containing, double agent regimen. Platinum can be either cisplatin or carboplatin, and the most commonly used drugs combined with platinum include paclitaxel, docetaxel, gemcitabine, and vinorelbine; other drugs such as irinotecan, etoposide, and vinblastine.

The arrival of immunotherapy with the PD-1 inhibitor pembrolizumab effectively changed the first-line standard. Pembrolizumab is very effective, with a long Duration of Response (DoR), however response rates remain suboptimal (approximately 45% in first line [Keytruda® Prescribing Information. 2020]). Most patients will eventually fail first line therapy and docetaxel remains a valid treatment option when NSCLC patients fail to respond to targeted or immune-based therapies or become refractory to such therapies.

For patients intolerant to platinum-containing regimens, platinum-free double-agent chemotherapy regimens are used as an alternative. For patients with an Eastern Cooperative Oncology Group score of 2 and elderly patients, single-agent or double agent regimens are recommended. Approval has been obtained in China for the single agent gefitinib to be used in first-line treatment of locally advanced or metastatic NSCLC patients with sensitive mutation of EGFR tyrosine kinase gene.

Second-line Therapy: Drugs used for second-line treatment include docetaxel, pemetrexed, EGFR-tyrosine kinase inhibitor (TKI) for EGFR mutant patients, and the checkpoint inhibitors (such as nivolumab and pembrolizumab).

Several second-line treatment drugs and regimens (docetaxel, pemetrexed, and ramucirumab combined with docetaxel) have been approved as single agents or combination for second-line therapy for locally advanced or metastatic NSCLC with EGFR wild type with limited efficacy, characterized by limited clinical improvement or overall survival (OS). EGFR wild type represents around 85% of western NSCLC population, and around 70% of Asian NSCLC population. Checkpoint inhibition with PD 1/programmed death-ligand 1 (PD-L1) inhibitors in combination with chemotherapy or other checkpoint inhibitors have moved into first line and are increasingly not an option for 2nd/3rd line. This has created a situation where docetaxel-based regimens have become standard-of-care in 2nd/3rd line NSCLC. Therefore, the evaluation of plinabulin combined with docetaxel versus docetaxel alone has become highly relevant.

Docetaxel, a taxane, binds to and stabilizes tubulin, thereby inhibiting microtubule disassembly resulting in cell cycle arrest at the G2/M phase and subsequent cell death. In patients with NSCLC, previously treated with a platinum-based chemotherapy, second-line therapy with docetaxel afforded a median OS in the range from 5.7 to 7.5 months (Fossella, 2000; Shepherd, 2000). The most common AEs included infections, neutropenia, anemia, febrile neutropenia (FN), hypersensitivity, thrombocytopenia, neuropathy, dysgeusia, dyspnea, constipation, anorexia, nail disorders, fluid retention, asthenia, pain, nausea, diarrhea, vomiting, mucositis, alopecia, skin reactions, and myalgia (Taxotere Prescribing Information, 2020). Since the approval of docetaxel in 1999 as the second-line treatment for advanced or metastatic NSCLC, other drugs, namely pemetrexed and erlotinib, have been approved for the same indication. However, despite the availability of newer treatments, patient survival has not improved over that achieved with docetaxel. The OS in these studies was found to remain in the range of 5.6 to 8.3 months (Hanna et al., 2004; Kim et al., 2008; Shepherd et al., 2005).

A retrospective analysis of the plinabulin Phase 2 study suggests that plinabulin prolongs survival in NSCLC patients with measurable lung tumors. The expectation is that patients with a measurable lung lesion may still harbor antigens that are immunogenic, thus capable of still stimulating the immune system. Docetaxel treatment is expected to release these immunogens and plinabulin is expected to enhance presentation of these immunogens via dendritic cell activation, to the T-cell repertoire.

This plinabulin study investigates the efficacy and safety of plinabulin and docetaxel combination in patients with EGFR wild type NSCLC and progressing tumors requiring second- or third- line therapy for advanced or metastatic disease after failing a platinum-containing regimen. The primary endpoint is OS, with docetaxel monotherapy as an active comparator.

Being tested
Docetaxel + Plinabulin (DP), Docetaxel (D)
Medical subject headings
Carcinoma, Non-Small-Cell Lung

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Docetaxel + Plinabulin (DP)Drug

    Also called BPI-2358, NPI-2358

    Docetaxel 75 mg/m2 IV + Plinabulin 30 mg/m2

  • Docetaxel (D)Drug

    Also called Taxotere

    Docetaxel 75 mg/m2 IV

Study groups in NCT02504489
Study groupRoleWhat they receive
Docetaxel (D)Active comparatorA treatment cycle is 21 days. Treatment will be repeated until disease progression is detected by imaging studies or unacceptable toxicities are encountered. On Day 1, all patients will receive docetaxel 75 mg/m2 by intravenous (IV) infusion over 1 hour. Oral dexamethasone (16 mg, given as 8 mg twice daily) will be given on the day prior to, the day of (Day 1), and the day following docetaxel infusion (Day 2). Antiemetic prophylaxis will be administered according to institutional guideline for docetaxel. Institutional guideline/practice should be followed in the event of infusion/hypersensitivity reaction. Diphenhydramine and dexamethasone infusion may be administered in the event of infusion reaction.
Receives: Drug: Docetaxel (D)
Docetaxel + Plinabulin (DP)ExperimentalThe treatment regimen for Docetaxel (D) will be followed for this arm. In addition, on Days 1 and 8 of the 21 day cycle, patients will receive Plinabulin (P) administered via IV infusion over 60 minutes. On Day 1, the infusion begins 2 hours from the starting time of docetaxel infusion, i.e, approximately 60 minutes from the end of docetaxel infusion. On Day 8, patients must be given an anti-emetic prophylactically before the plinabulin infusion. If emesis persists after Day 8, with a grade >1, plinabulin will be reduced to 20 mg/m2. Patients from the DP Arm who stop treatment with docetaxel due to toxicity or another medically acceptable reason, may continue treatment with plinabulin alone as previously described.
Receives: Drug: Docetaxel + Plinabulin (DP); Drug: Docetaxel (D)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Overall Survival

    Overall survival is defined as the time (days) from the date of randomization to the date of death due to any cause (i.e., Date of death - date of randomization +1).

    Measured: The time (Days) from the date of randomization to the date of death, up to 48 months

Secondary outcomes (13)
  1. ORR

    Overall response rate

    Measured: up to 2 years after study Initiation

  2. PFS

    Progress-free survival

    Measured: Up to 48 months after study initiation.

  3. Severe Neutropenia

    Percent of patients without severe neutropenia on Day 8 of Cycle 1

    Measured: Day 8 of Cycle 1 (±1 day)

  4. Month 24 OS Rate

    To compare 24-month overall survival rate

    Measured: up to 24months after study initiation

  5. Month 36 OS Rate

    To compare 36-month overall survival rate

    Measured: up to 36 months after study initiation

  6. DoR

    Duration of response

    Measured: Up to 2 years after study initiation.

  7. Change From Baseline in EORTC QLQ-C30 Global Health Status / Quality of Life Score

    The European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) Global Health Status / Quality of Life scale was used.

    The Global Health Status / Quality of Life scale is transformed to a 0-100 scale according to the EORTC scoring manual.

    Minimum value: 0 Maximum value: 100 Higher scores indicate better quality of life The reported values represent the mean change from baseline to end of treatment (end of treatment score minus baseline score).

    Measured: Baseline and End of Treatment (Last study assessment prior to treatment discontinuation), assessed up to 2 years after study initiation.

  8. Q-TWiST

    To compare the mean difference in quality-adjusted time without symptoms of disease and toxicity

    Measured: up to 2 years after study initiation.

  9. QoL (QLQ-LC13)

    EORTC QLQ C30/QLQ LC13, this instrument consists of one multi-item dyspnea scale and several single item symptom scales (e.g. pain, coughing, sore mouth, dysphagia, peripheral neuropathy, alopecia and hemoptysis).

    All LC13 symptom scales were scored according to the EORTC QLQ C30/QLQ LC13 scoring manuals. On this 0-100 scale, higher scores represent a higher level of symptoms (worse outcome).

    The QLQ LC13 Symptom Combined Score used for this outcome is the average of all available LC13 symptom scale scores, if all 3 dyspnea items are non-missing, the dyspnea scale score and all other symptom scales are calculated and the Symptom Combined Score is the average of all available scales.

    The reported LSMeans (SE) and LSMeans differences (95% CI) are based on this 0-100 Symptom Combined Score, where 0 indicates no lung cancer-related symptoms and 100 indicates the highest level of symptoms.

    Measured: Up to 2 years after study initiation.

  10. Proportion of Patients Who Received Docetaxel

    To compare proportion of patients who received docetaxel >8 cycles, >10 cycles, and >12 cycles

    Measured: Up to 29 cycles

  11. Month 18 OS Rate

    To compare 18-month overall survival rate

    Measured: up to 18 months after study initiation

  12. Analysis of the Relative Dose Intensity of Docetaxel Over the First 4, 6, 8, 10, 12 Cycles

    Relative Dose Intensity (RDI) was defined as the ratio of the actual delivered dose intensity to the planned dose intensity of docetaxel. Dose intensity was calculated as the total dose (mg/m²) divided by the actual cycle duration (days) and normalized to the planned 21-day treatment cycle. Thus, RDI = [(Actual dose / actual duration) / (Planned dose / 21 days)]. RDI values were summarized as mean (SD), median, and range per treatment group after 4, 6, 8, 10, and 12 cycles."

    Note: Analysis population: ITT (Docetaxel [D] n=281; Docetaxel + Plinabulin [DP] n=278). Means (SD) were calculated using participants with available data at each duration; therefore, the number analyzed varies by row.

    Measured: First Cycle 1 Day 1 to the end of Cycle 12 (approximately up to 36 weeks)

  13. Month 12 OS Rate

    To compare 12-month overall survival rate

    Measured: up to 12 months after study initiation

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Jul 2015 (estimated)
  2. Study startDec 2015
  3. Primary completion21 Jul 2021
  4. Study completion30 Oct 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
559 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02504489
Sponsor's protocol ID
BPI-2358-103
Acronym
DUBLIN-3
Status last verified
Dec 2025
First submitted
16 Jul 2015
Last updated
19 May 2026
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No

Publications

  • Han B, Feinstein T, Shi Y, Chen G, Yao Y, Hu C, Shi J, Feng J, Wu H, Cheng Y, Guo QS, Jie Z, Ye F, Zhang Y, Liu Z, Mao W, Zhang L, Lu J, Zhao J, Bazhenova L, Ruiz J, Kloecker GH, Sujith KR, Oliff IA, Wong M, Liu B, Wu Y, Huang L, Sun Y; DUBLIN-3 study group. Plinabulin plus docetaxel versus docetaxel in patients with non-small-cell lung cancer after disease progression on platinum-based regimen (DUBLIN-3): a phase 3, international, multicentre, single-blind, parallel group, randomised controlled trial. Lancet Respir Med. 2024 Oct;12(10):775-786. doi: 10.1016/S2213-2600(24)00178-4. Epub 2024 Sep 9.

    PubMed 39265599

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Docetaxel + Plinabulin (DP) and Docetaxel (D) in people with Non-Small Cell Lung Cancer, run by BeyondSpring Pharmaceuticals Inc. at 57 sites in 3 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 21 inclusion and 18 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 57 sites in China, United States, Australia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 19 May 2026). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Overall Survival (time frame: The time (Days) from the date of randomization to the date of death, up to 48 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02504489, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 May 2026.

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