Skip to content

A Phase II study of Pemetrexed/Bevacizumab in patients ineligible for platinum-based chemotherapy with untreated Advanced Non-squamous non-small-cell lung cancer (ALCT003)

A Phase II study of Pemetrexed/Bevacizumab in patients ineligible for platinum-based chemotherapy with untreated Advanced Non-squamous non-small-cell lung cancer (ALCT003) - A Phase II study of PEM/Bev in patients ineligible for platinum-based chemotherapy with untreated Advanced Non-sq NSCLC (ALCT003)

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000010805
Enrollment
25
Registered
2013-05-26
Start date
2013-04-25
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-squamous Non-small cell lung cancer

Interventions

Pemetrexed plus Bevacizumab as front-line treatment

Sponsors

Department of Respiratory Medicine Kyorin Univercity Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) histologically or cytologically confirmed 2)newly diagnosed stage IIIB,IV 3)recurrent NSCLC for which they had not received chemotherapy 4)measurable or nonmeasurable disease as defined by Response Evaluation Criteria in Solid Tumors 5)age 20-69 Performance status:2 age 70-74 Performance status:1-2 age 75≤ Performance status:0-2 Patients ineligible for platinum-based chemotherapy 6)adequate hematologic, hepatic, and renal functions 7)Patients expected to survive longer than at least three months 8)patients with a history of brain metastases after treatments more than a week ago 9)Patients who provide written informed consent

Exclusion criteria

Exclusion criteria: 1)active double cancer 2)clinically significant infectious disease 3)history of gross hemoptysis (2.5ml) 4)regular use of aspirin 5)history of diverticulitis or clinically significant diverticular disease 6)clinically significant cardiovascular disease and DVT 7)medically uncontrolled hypertension and diabetes 8)active or symptomatic interstitial lung disease 9)Patients with the plan of operation or thoracic irradiation 10)Patients with wound that has not quite healed 11)pregnancy or lactation

Design outcomes

Primary

MeasureTime frame
progression free surviaval

Secondary

MeasureTime frame
Response rate, Overall survival, QOL,Time to response,Safety,evaluation of thymidylate synthase protein expression

Countries

Japan

Contacts

Public ContactTakuma Yokoyama

Kyorin Univercity Hospital Department of Respiratory Medicine

taku@ks.kyorin-u.ac.jp0422-47-5511

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026