ClinicalTrials.gg
Status unknownNCT02974933Updated Feb 17, 2017

Apatinib Mesylate Combined With Pemetrexed in the Treatment of Pretreated Advanced Non-squamous Non-small Cell Lung Cancer

A Phase 2 interventional study of Apatinib combined with pemetrexed in Nonsmall Cell Lung Cancer, sponsored by Wuling Ou. Status unknown at 1 site in China. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2017-02-17.

Sponsored by Wuling Ou · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Feb 2017), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
48
Allocation
Not applicable
Ages
18 Years to 70 Years
Sex
All
01

Study summary

The purpose of this study is to evaluate the efficacy of apatinib mesylate combined with pemetrexed alone in advanced non-small cell lung cancer patients in the second or second line of treatment of progression-free survival

Read the detailed description

It is a one-arm study. The progression-free survival will be evaluated.

02

Conditions studied

  • Nonsmall Cell Lung Cancer

Keywords

  • apatinib
  • pemetrexed
  • NSCLC
03

In context

Carcinoma, Non-Small-Cell Lung

6,645 studies on the registry are indexed under Carcinoma, Non-Small-Cell Lung; 1,665 are open to participants now.

This study's planned enrollment of 48 is below the median of 62 across 5,327 interventional studies indexed under Carcinoma, Non-Small-Cell Lung.

Browse Carcinoma, Non-Small-Cell Lung studies →

Lead sponsor

This is the only study on the registry with Wuling Ou as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Aged from 18 years to 70years.
  2. Histologically or cytologically confirmed non-squamous non-small cell lung cancer(stage IIIB/IV).
  3. Measurable lesions as defined by RECIST criteria.
  4. Locally advanced lung cancer cannot treat with surgery, recurrent or metastatic lung cancer
  5. ECOG performance status (PS) of 0 to 1.
  6. Life expectancy ≥3 months.
  7. Informed consent.

Exclusion criteria

Exclusion Criteria:

  1. Squamous carcinoma (including adeno-squamous carcinoma), small cell lung cancer.
  2. Newly diagnosed Central Nervous System (CNS) metastases that have not yet been definitively treated with surgery and/or radiation.
  3. Tumor invade big vessels or close to big vessels (less than 5mm)
  4. Obvious cavity or necrosis formed in the tumor
  5. Uncontrolled hypertension
  6. Myocardial ischemia or infarction more than stage II, cardiac insufficiency.
  7. Abnormal coagulation (INR>1.5 or PT>ULN+4, or APTT>1.5 ULN), bleeding tendency or receiving coagulation therapy
  8. The active HBV or HCV infection
  9. History of other malignancies except cured basal cell carcinoma of skin and carcinoma in-situ of uterine cervix.
  10. Hemoptysis, more than 2.5ml daily
  11. Thrombosis in 12 months, including pulmonary thrombosis, stoke, or deep venous thrombosis.
  12. Unhealed bone fracture or wound for long time
  13. Received big surgery, had bone fracture or ulcer in 4 weeks.
  14. Urine protein≥++, or urine protein in 24 hours≥1.0g
  15. Use of CYP3A4 inhibitor within 7 days or CYP3A4 inducer within 12 days prior to enrollment
  16. Have received prior treatment with VEGFR TKI (Bevacizumab is permitted).
  17. Pregnant or lactating woman, or woman unwilling to practice contraception during the study.
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
48 participants (estimated)

Study arms

  • Experimental
    apatinib

    combined with pemetrexed

    Drug: Apatinib combined with pemetrexed

Interventions

  • DrugApatinib combined with pemetrexed

    For those pretreated non-squamous non-small cell lung cancer, treat with apatinib 500mg Qd, po.combined with pemetrexed continue until disease progression

06

What researchers measure

Primary outcomes

  1. progression free survival

    evaluation per 28 days

    Time frame: 4 weeks

Secondary outcomes

  1. Overall Survival

    evaluation per 28 days

    Time frame: 4 weeks

  2. disease control rate

    evaluation per 28 days

    Time frame: 4 weeks

  3. objective response rate

    evaluation per 28 days

    Time frame: 4 weeks

  4. Adverse Event

    evaluation per 28 days

    Time frame: 4 weeks

07

Study locations

1 of 1 sites recruiting
  • Ou wuling
    Wuhan, Hubei 430079, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 17, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02974933
Lead sponsor
Wuling Ou
Collaborators
Jiangsu HengRui Medicine Co., Ltd., Hubei Clinical Research Collaboration Group
Responsible party
Wuling Ou (Deputy Chief Physician, Hubei Cancer Hospital) — Sponsor-investigator
First posted
Nov 29, 2016
Start date
Nov 2016
Primary completion
Nov 2017 (estimated)
Completion
Nov 2018 (estimated)
Last update
Feb 17, 2017

Study contacts

Ou Wu Ling, MD
Contact
609700817@qq.com

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Feb 2017. You cannot join it, but the record below documents what was studied.

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