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Non-Small Cell Lung CancerPhase 3PACIFICNCT02125461

A Global Study to Assess the Effects of MEDI4736 Following Concurrent Chemoradiation in Patients With Stage III Unresectable Non-Small Cell Lung Cancer

A Phase 3 study testing MEDI4736 in people with Non-Small Cell Lung Cancer, run by AstraZeneca at 236 sites in 26 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

A Global Study to Assess the Effects of MEDI4736 following concurrent chemoradiation in Patients with Stage III Unresectable Non-Small Cell Lung Cancer. Read more about this study

Who is it for?
Ages 18 to 130 years
Conditions the study is for
Non-Small Cell Lung Cancer
What is being tested?
MEDI4736
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
713 participants
Where
236 sitesin 26 countries
Study dates
7 May 2014to 24 Aug 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 to 130 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age at least 18 years.
  • Documented evidence of NSCLC (locally advanced, unresectable, Stage III)
  • Patients must have received at least 2 cycles of platinum-based chemotherapy concurrent with radiation therapy.
  • World Health Organisation (WHO) Performance Status of 0 to 1.
  • Estimated life expectancy of more than 12 weeks.

Who cannot join

  • Prior exposure to any anti-PD-1 or anti-PD-L1 antibody.
  • Active or prior autoimmune disease or history of immunodeficiency.
  • Evidence of severe or uncontrolled systemic diseases, including active bleeding diatheses or active infections including hepatitis B, C and HIV.
  • Evidence of uncontrolled illness such as symptomatic congestive heart failure, uncontrolled hypertension or unstable angina pectoris.
  • Any unresolved toxicity CTCAE >Grade 2 from the prior chemoradiation therapy.
  • Active or prior documented inflammatory bowel disease (eg, Crohn's disease, ulcerative colitis).

Trial locations and contacts

236 sites in 26 countries.

236 sites in 26 countries

United States60 sites
  • Research Site

    Atlanta, Georgia, 30318

  • Research Site

    Atlanta, Georgia, 30322

  • Research Site

    Austin, Texas, 78731

  • Research Site

    Baltimore, Maryland, 21287

  • Research Site

    Blue Ash, Ohio, 45242

  • Research Site

    Boston, Massachusetts, 02215

  • Research Site

    Burlington, North Carolina, 27215

  • Research Site

    Chandler, Arizona, 85224

  • Research Site

    Charlotte, North Carolina, 28204

  • Research Site

    Chattanooga, Tennessee, 37404

  • Research Site

    Dallas, Texas, 75231

  • Research Site

    Dallas, Texas, 75246

  • Research Site

    Easley, South Carolina, 29640

  • Research Site

    Fairfax, Virginia, 22031

  • Research Site

    Fort Gordon, Georgia, 30905

  • Research Site

    Fort Myers, Florida, 33901

  • Research Site

    Fort Worth, Texas, 76104

  • Research Site

    Fullerton, California, 92835

  • Research Site

    Goodyear, Arizona, 85338

  • Research Site

    Hackensack, New Jersey, 07601

  • Research Site

    Hazard, Kentucky, 41701

  • Research Site

    Houston, Texas, 77030

  • Research Site

    Jacksonville, Florida, 32207

  • Research Site

    Jonesboro, Arkansas, 72405

  • Research Site

    Lake Success, New York, 11041

  • Research Site

    Lansing, Michigan, 48910

  • Research Site

    Lawrenceville, Georgia, 30046

  • Research Site

    Lincoln, Nebraska, 68510

  • Research Site

    Los Angeles, California, 90095

  • Research Site

    Marietta, Georgia, 30060

  • Research Site

    Miami Beach, Florida, 33140

  • Research Site

    Minneapolis, Minnesota, 55426

  • Research Site

    Nashville, Tennessee, 37203

  • Research Site

    Nashville, Tennessee, 37232-8805

  • Research Site

    Norwich, Connecticut, 06360

  • Research Site

    Orlando, Florida, 32804

  • Research Site

    Oxnard, California, 93030

  • Research Site

    Pinehurst, North Carolina, 28374

  • Research Site

    Port Saint Lucie, Florida, 34952

  • Research Site

    Rockville, Maryland, 20850

  • Research Site

    Rosedale, Maryland, 21237

  • Research Site

    Sacramento, California, 95816

  • Research Site

    Salisbury, Maryland, 21801

  • Research Site

    Salt Lake City, Utah, 84106

  • Research Site

    San Diego, California, 92123

  • Research Site

    Santa Rosa, California, 95403

  • Research Site

    Spokane, Washington, 99208

  • Research Site

    Spokane, Washington, 99218

  • Research Site

    Springdale, Arkansas, 72762

  • Research Site

    St Louis, Missouri, 63110

  • Research Site

    St. Petersburg, Florida, 33705

  • Research Site

    Tampa, Florida, 33612

  • Research Site

    The Bronx, New York, 10461

  • Research Site

    Topeka, Kansas, 66606

  • Research Site

    Towson, Maryland, 21204

  • Research Site

    Tyler, Texas, 75702

  • Research Site

    Vancouver, Washington, 98684

  • Research Site

    Washington D.C., District of Columbia, 20007

  • Research Site

    Waterloo, Iowa, 50701

  • Research Site

    Winston-Salem, North Carolina, 27103

Other trials in United States

Japan29 sites
  • Research Site

    Bunkyō City, 113-8431

  • Research Site

    Bunkyō City, 113-8603

  • Research Site

    Chūōku, 104-0045

  • Research Site

    Fukuoka, 812-8582

  • Research Site

    Habikino-shi, 583-8588

  • Research Site

    Hidaka-shi, 350-1298

  • Research Site

    Hirakata-shi, 573-1191

  • Research Site

    Hiroshima, 730-8518

  • Research Site

    Kanazawa, 920-8641

  • Research Site

    Kashiwa, 277-8577

  • Research Site

    Kitaadachi-gun, 362-0806

  • Research Site

    Kurume-shi, 830-0011

  • Research Site

    Matsuyama, 791-0280

  • Research Site

    Nagoya, 460-0001

  • Research Site

    Natori-shi, 981-1293

  • Research Site

    Okayama, 700-8558

  • Research Site

    Osaka, 541-8567

  • Research Site

    Ota-shi, 373-8550

  • Research Site

    Sagamihara-shi, 252-0375

  • Research Site

    Sakaishi, 591-8555

  • Research Site

    Sapporo, 003-0804

  • Research Site

    Sayama, 589-8511

  • Research Site

    Sendai, 980-0873

  • Research Site

    Shinjuku-ku, 162-8655

  • Research Site

    Sunto-gun, 411-8777

  • Research Site

    Takatsuki-shi, 569-8686

  • Research Site

    Ube-shi, 755-0241

  • Research Site

    Yokohama, 236-0051

  • Research Site

    Yokohama, 241-8515

Other trials in Japan

Spain17 sites
  • Research Site

    Alicante, 03010

  • Research Site

    Barcelona, 08003

  • Research Site

    Barcelona, 08041

  • Research Site

    Barcelona, 08908

  • Research Site

    Donostia / San Sebastian, 20014

  • Research Site

    Girona, 17007

  • Research Site

    Lleida, 25198

  • Research Site

    Madrid, 28005

  • Research Site

    Madrid, 28007

  • Research Site

    Madrid, 28041

  • Research Site

    Madrid, 28046

  • Research Site

    Madrid, 28050

  • Research Site

    Seville, 41009

  • Research Site

    Seville, 41013

  • Research Site

    Valencia, 46014

  • Research Site

    Valencia, 46026

  • Research Site

    Zaragoza, 50009

Other trials in Spain

France14 sites
  • Research Site

    Avignon, 84918

  • Research Site

    Bayonne, 64100

  • Research Site

    Brest, 29609

  • Research Site

    Lille, 59037

  • Research Site

    Lyon, 69008

  • Research Site

    Marseille, 13915

  • Research Site

    Montpellier, 34295

  • Research Site

    Nantes, 44202

  • Research Site

    Nice, 06100

  • Research Site

    Pau, 6400

  • Research Site

    Rennes, 35033

  • Research Site

    Saint-Herblain, 44805

  • Research Site

    Toulouse, 31000

  • Research Site

    Villejuif, 94805

Other trials in France

Australia13 sites
  • Research Site

    Bedford Park, 5042

  • Research Site

    Bendigo, 3550

  • Research Site

    Box Hill, 3128

  • Research Site

    Clayton, 3168

  • Research Site

    Heidelberg, 3084

  • Research Site

    Herston, 4029

  • Research Site

    Kogarah, 2217

  • Research Site

    Launceston, 7250

  • Research Site

    Nedlands, 6009

  • Research Site

    Port Macquarie, 2444

  • Research Site

    Randwick, 2031

  • Research Site

    Westmead, 2145

  • Research Site

    Woolloongabba, 4102

Other trials in Australia

Germany10 sites
  • Research Site

    Berlin, 10967

  • Research Site

    Berlin, 12351

  • Research Site

    Esslingen am Neckar, 73730

  • Research Site

    Großhansdorf, 20927

  • Research Site

    Hamburg, 20251

  • Research Site

    Hamburg, 22081

  • Research Site

    Löwenstein, 74245

  • Research Site

    Recklinghausen, 45659

  • Research Site

    Regensburg, 93053

  • Research Site

    Villingen-Schwenningen, 78052

Other trials in Germany

South Korea10 sites
  • Research Site

    Busan, 49201

  • Research Site

    Cheongju-si, 361-711

  • Research Site

    Hwasun-gun, 58128

  • Research Site

    Incheon, UNK

  • Research Site

    Seongnam-si, 13620

  • Research Site

    Seoul, 02841

  • Research Site

    Seoul, 03722

  • Research Site

    Seoul, 05505

  • Research Site

    Seoul, 06351

  • Research Site

    Suwon, 16247

Other trials in South Korea

Canada9 sites
  • Research Site

    Barrie, Ontario, L4M 6M2

  • Research Site

    Calgary, Alberta, T2N 4N2

  • Research Site

    Edmonton, Alberta, T6G 1Z2

  • Research Site

    London, Ontario, N6A 4L6

  • Research Site

    Newmarket, Ontario, L3Y 2P9

  • Research Site

    Oshawa, Ontario, L1G 2B9

  • Research Site

    Toronto, Ontario, M4N 3M5

  • Research Site

    Toronto, M5G 2M9

  • Research Site

    Vancouver, British Columbia, V5Z 4E6

Other trials in Canada

Italy9 sites
  • Research Site

    Aviano, 33081

  • Research Site

    Catania, 95123

  • Research Site

    Cremona, 26100

  • Research Site

    Lecce, 73100

  • Research Site

    Milan, 20132

  • Research Site

    Milan, 20133

  • Research Site

    Naples, 80138

  • Research Site

    Pisa, 56126

  • Research Site

    Roma, 00144

Other trials in Italy

Turkey (Türkiye)7 sites
  • Research Site

    Adana, 01130

  • Research Site

    Ankara, 06490

  • Research Site

    Istanbul, 34030

  • Research Site

    Istanbul, 34844

  • Research Site

    Izmir, 35100

  • Research Site

    Konya, 42080

  • Research Site

    Malatya, 44280

Other trials in Turkey (Türkiye)

Netherlands6 sites
  • Research Site

    Amsterdam, 1066 CX

  • Research Site

    Amsterdam, 1081 HV

  • Research Site

    Breda, 4818 CK

  • Research Site

    Eindhoven, 5623EJ

  • Research Site

    Rotterdam, 3015 CE

  • Research Site

    Tilburg, 5022 GC

Other trials in Netherlands

Belgium5 sites
  • Research Site

    Aalst, 9300

  • Research Site

    Gilly, 6060

  • Research Site

    Leuven, 3000

  • Research Site

    Libramont-Chevigny, 6800

  • Research Site

    Liège, 4000

Other trials in Belgium

Greece5 sites
  • Research Site

    Athens, 11527

  • Research Site

    Heraklion, 71110

  • Research Site

    Pátrai, 26500

  • Research Site

    Thessaloniki, 54645

  • Research Site

    Thessaloniki, 57010

Other trials in Greece

Taiwan5 sites
  • Research Site

    Taichung, 40447

  • Research Site

    Taipei, 110

  • Research Site

    Taipei, 112

  • Research Site

    Taipei, 23561

  • Research Site

    Taipei

Other trials in Taiwan

Hungary4 sites
  • Research Site

    Budapest, 1083

  • Research Site

    Budapest, 1121

  • Research Site

    Gyula, 5703

  • Research Site

    Miskolc, 3529

Other trials in Hungary

Mexico4 sites
  • Research Site

    Cuautitlán Izcalli, 54769

  • Research Site

    Monterrey, 64460

  • Research Site

    Oaxaca City, 68000

  • Research Site

    Orizaba, 94300

Other trials in Mexico

Slovakia4 sites
  • Research Site

    Bardejov, 08501

  • Research Site

    Košice, 041 91

  • Research Site

    Nové Zámky, 94002

  • Research Site

    Trnava, 91775

Other trials in Slovakia

Chile3 sites
  • Research Site

    Santiago, 7500000

  • Research Site

    Santiago, 8420383

  • Research Site

    Viña del Mar

Other trials in Chile

Poland3 sites
  • Research Site

    Gdansk, 80-952

  • Research Site

    Lublin, 20-362

  • Research Site

    Warsaw, 02-781

Other trials in Poland

Singapore3 sites
  • Research Site

    Singapore, 119074

  • Research Site

    Singapore, 169610

  • Research Site

    Singapore, 308433

Other trials in Singapore

South Africa3 sites
  • Research Site

    Cape Town, 7570

  • Research Site

    Pretoria, 0181

  • Research Site

    Vereeniging, 1930

Other trials in South Africa

Thailand3 sites
  • Research Site

    Bangkok, 10400

  • Research Site

    Hat Yai, 90110

  • Research Site

    Muang, 50200

Other trials in Thailand

United Kingdom3 sites
  • Research Site

    Glasgow, G12 0YN

  • Research Site

    Manchester, M20 4BX

  • Research Site

    Truro, TR1 3LJ

Other trials in United Kingdom

Vietnam3 sites
  • Research Site

    Hanoi, 100000

  • Research Site

    Hanoi, 10000

  • Research Site

    Ho Chi Minh City, 700000

Other trials in Vietnam

Israel2 sites
  • Research Site

    Haifa, 31096

  • Research Site

    Jerusalem, 91120

Other trials in Israel

Peru2 sites
  • Research Site

    Lima, 41

  • Research Site

    Lima, LIMA 27

Other trials in Peru

About this study

Official title: A Phase III, Randomised, Double-blind, Placebo-controlled, Multi-centre, International Study of MEDI4736 as Sequential Therapy in Patients With Locally Advanced, Unresectable Non-Small Cell Lung Cancer (Stage III) Who Have Not Progressed Following Definitive, Platinum-based, Concurrent Chemoradiation Therapy (PACIFIC)

A Global Study to Assess the Effects of MEDI4736 following concurrent chemoradiation in Patients with Stage III Unresectable Non-Small Cell Lung Cancer.

Read the detailed description

A Phase III, Randomised, Double-blind, Placebo-controlled, Multi-centre, International Study of MEDI4736 as Sequential Therapy in Patients with Locally Advanced, Unresectable Non-Small Cell Lung Cancer (Stage III) Who Have Not Progressed Following Definitive, Platinum-based, Concurrent Chemoradiation Therapy (PACIFIC)

Being tested
MEDI4736, PLACEBO
Keywords
Locally advanced, Unresectable Non-Small Cell Lung Cancer, MEDI4736, PD-L1, Stage III Non-Small Cell Lung Cancer, Chemoradiation, Immune-mediated cancer therapy
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.

  • MEDI4736Drug

    MEDI4736 by intravenous infusion. Treatment from Day 1 for a maximum of 12 months or study drug withdrawal if this occurs earlier . The 2:1 ratio (MEDI4736 to placebo).

  • PLACEBOOther

    PLACEBO by intravenous infusion. Treatment from Day 1 for a maximum of 12 months or study drug withdrawal if this occurs earlier . The 2:1 ratio (MEDI4736 to placebo).

Study groups in NCT02125461
Study groupRoleWhat they receive
MEDI4736ExperimentalMEDI4736 (intravenous infusion)
Receives: Drug: MEDI4736
PLACEBOPlacebo comparatorPlacebo (matching placebo for intravenous infusion)
Receives: Other: PLACEBO

What is being measured

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

  1. Progression Free Survival Based on Blinded Independent Central Review (BICR) According to Response Evaluation Criteria in Solid Tumors (RECIST 1.1)

    PFS was defined as the time from randomization until the date of objective disease progression (RECIST 1.1) or death (by any cause in the absence of progression). Progression was defined using RECIST 1.1 as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions. PFS was calculated using the Kaplan-Meier technique.

    Measured: Tumor scans performed at baseline then every ~8 weeks up to 48 weeks, then every ~12 weeks thereafter until confirmed disease progression. Assessed until 13 Feb 2017 DCO; up to a maximum of approximately 3 years.

  2. Overall Survival

    OS was defined as the time from the date of randomization until death due to any cause. OS was calculated using the Kaplan-Meier technique.

    Measured: From baseline until death due to any cause. Assessed until 22 Mar 2018 DCO; up to a maximum of approximately 4 years.

Secondary outcomes (11)
  1. Objective Response Rate (ORR) Based on BICR Assesments According to RECIST 1.1

    ORR was defined as the percentage of patients with at least one visit response of Complete Response (CR) or Partial Response (PR) per RECIST 1.1 for target lesions: CR: Disappearance of all target lesions; PR: >=30% decrease in the sum of the longest diameter of target lesions; OR = CR + PR.

    Measured: Tumor scans performed at baseline then every ~8 weeks up to 48 weeks, then every ~ 12 weeks thereafter until confirmed disease progression. Assessed until 22 Mar 2018 DCO; up to a maximum of approximately 4 years.

  2. Duration of Response (DoR) Based on BICR Assessments According to RECIST 1.1

    DoR was defined as the time from date for first documented response of CR or PR until the first documented response of progression per RECIST 1.1 or death in the absence of progression. DoR was calculated using the Kaplan-Meier technique.

    Measured: Tumor scans performed at baseline then every ~8 weeks up to 48 weeks, then every ~ 12 weeks thereafter until confirmed disease progression. Assessed until 22 Mar 2018 DCO; up to a maximum of approximately 4 years.

  3. Proportion of Patients Alive and Progression Free at 12 Months From (APF12) Based on BICR Assessments According to RECIST 1.1

    APF12 was defined as the percentage of patients who were alive and progression free per RECIST 1.1 at 12 months after randomization per Kaplan-Meier estimate of PFS at 12 months.

    Measured: Tumor scans performed at baseline then every ~8 weeks up to 48 weeks, then every ~ 12 weeks thereafter until confirmed disease progression. Assessed until 13 Feb 2017 DCO; up to a maximum of approximately 3 years.

  4. Proportion of Patients Alive and Progression Free at 18 Months From (APF18) Based on BICR Assessments According to RECIST 1.1

    APF18 was defined as the percentage of patients who were alive and progression free per RECIST 1.1 at 18 months after randomization per the Kaplan-Meier estimate of PFS at 18 months.

    Measured: Tumor scans performed at baseline then every ~8 weeks up to 48 weeks, then every ~ 12 weeks thereafter until confirmed disease progression. Assessed until 13 Feb 2017 DCO; up to a maximum of approximately 3 years.

  5. Time to Death or Distant Metastasis (TTDM) Based on BICR Assessments According to RECIST 1.1

    TTDM was defined as the time from the date of randomization until the first date of distant metastasis or death in the absence of distant metastasis. Distant metastasis was defined as any new lesion that was outside of the radiation field according to RECIST 1.1 or proven by biopsy. TTDM was calculated using the Kaplan-Meier technique.

    Measured: Tumor scans performed at baseline then every ~8 weeks up to 48 weeks, then every ~ 12 weeks thereafter until confirmed disease progression. Assessed until 22 Mar 2018 DCO; up to a maximum of approximately 4 years.

  6. Percentage of Patients Alive at 24 Months (OS24)

    OS24 was defined as the percentage of patients who were alive at 24 months after randomization per the Kaplan-Meier estimate of OS at 24 months.

    Measured: From baseline until death due to any cause. Assessed until 22 Mar 2018 DCO; up to a maximum of approximately 4 years.

  7. Time to Second Progression or Death (PFS2)

    PFS2 was defined as the time from randomization to the time of the second progression or death. The date of second progression was recorded by the investigator and defined according to local standard clinical practice, and could have involved any of the following: objective radiological, symptomatic progression, or death. RECIST assessments were not collected for assessment of PFS2. PFS2 was calculated using the Kaplan-Meier technique.

    Measured: Following confirmed progression, patients were assessed every ~12 weeks until second disease progression. Assessed until 22 Mar 2018 DCO; up to a maximum of approximately 4 years.

  8. Time to Deterioration of Global Health Status / Health-Related Quality of Life (HRQoL), Assessed Using European Organization for Research and Treatment of Cancer 30-Item Core Quality of Life Questionnaire (EORTC QLQ-C30)

    Global health status/HRQoL was assessed using the EORTC QLQ-C30 global QoL scale which includes 2 items from the QLQ-C30: "How would you rate your overall health during the past week?" (Item 29) and "How would you rate your overall QoL during the past week?" (Item 30). Scores from 0 to 100 were derived for each item with higher scores indicating a better health status. Time to deterioration for global health status/HRQoL was defined as time from randomization until the date of first clinically meaningful deterioration (a decrease in global health status/HRQoL from baseline of ≥10) or death (by any cause) in the absence of a clinically meaningful deterioration. Time to deterioration was calculated using the Kaplan-Meier technique.

    Measured: At baseline, every 4 weeks for first 8 weeks, then every ~8 weeks until 48 weeks, then every ~12 weeks thereafter until confirmed disease progression. Assessed until 22 Mar 2018 DCO; up to a maximum of approximately 4 years.

  9. Time to Deterioration of Primary Patient-Reported Outcome (PRO) Symptoms, Assessed Using European Organization for Research and Treatment of Cancer QoL Lung Cancer Module (EORTC QLQ-LC13)

    The EORTC QLQ-LC13 is a lung cancer specific module from the EORTC comprising 13 questions to assess lung cancer symptoms (cough, hemoptysis, dyspnea, chest pain, arm/shoulder pain, and other pain), treatment related side-effects (sore mouth, dysphagia, peripheral neuropathy and alopecia) and pain medication. Scores from 0 to 100 were derived for each symptom item with higher scores representing greater symptom severity. Time to symptom deterioration was defined as time from randomization until the date of first clinically meaningful symptom deterioration (an increase in the score from baseline of ≥10) or death (by any cause) in the absence of a clinically meaningful symptom deterioration. Results are presented for time to deterioration in the following PRO endpoints identified as primary for EORTC QLQ-LC13: dyspnea, cough, hemoptysis and chest pain. Time to deterioration was calculated using the Kaplan-Meier technique.

    Measured: At baseline, every 4 weeks for first 8 weeks, then every ~8 weeks until 48 weeks, then every ~12 weeks thereafter until confirmed disease progression. Assessed until 22 Mar 2018 DCO; up to a maximum of approximately 4 years.

  10. Pharmacokinetics (PK) of Durvalumab; Peak and Trough Serum Concentrations

    To evaluate PK, blood samples were collected pre-dose and post-dose and trough and peak serum concentrations of durvalumab, respectively, were determined. Pre-dose samples were taken within 60 minutes before infusion and post-dose samples were taken within 10 minutes after the end of infusion.

    Measured: Samples were collected pre-dose on Day 1 (Week 0), Week 8, Week 24 and Week 48, and post-dose on Day 1 (Week 0) and Week 24. Analysis performed at 22 Mar 2018 DCO.

  11. Number of Patients With Anti-Drug Antibody (ADA) Response to Durvalumab

    ADA positive post-baseline only was also referred to as treatment-induced ADA positive. Treatment-boosted ADA was defined as baseline positive ADA titer that was boosted by ≥4-fold following drug administration. Persistently positive was defined as positive at ≥2 post-baseline assessments (with ≥16 weeks between first and last positive) or positive at last post-baseline assessment. Transiently positive was defined as having at least 1 post-baseline ADA positive assessment and not fulfilling the conditions of persistently positive. Confirmed ADA positive samples were subsequently tested in a neutralizing antibody assay.

    Measured: Samples were collected pre-dose on Day 1 (Week 0), Week 8, Week 24 and Week 48. Analysis performed at 22 Mar 2018 DCO.

Timeline

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

  1. First posted29 Apr 2014 (estimated)
  2. Study start7 May 2014
  3. Primary completion13 Feb 2017
  4. Study completion24 Aug 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
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
713 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02125461
Sponsor's protocol ID
D4191C00001
Other IDs
2014-000336-42, 2014
Acronym
PACIFIC
Status last verified
Sep 2023
First submitted
25 Apr 2014
Last updated
10 Oct 2023
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal. All request will be evaluated as per the AZ disclosure commitment: https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure. Yes, indicates that AZ are accepting requests for IPD, but this does not mean all requests will be shared.

Publications

  • Brunetti L, Santo V, Pinato DJ, Citarella F, Orlando S, Acker F, Colella V, Ricciuti B, Naidoo J, Nassar A, Wakelee HA, Takada K, Naqash AR, Garassino MC, Greco C, Ramella S, Pantano F, Tonini G, Vincenzi B, Arlunno B, Remon J, Parisi C, Planchard D, Besse B, Desilets A, Routy B, Elkrief A, Barlesi F, Derosa L, Cortellini A. Differential impact of proton pump inhibitors and antibiotics on immunotherapy efficacy after chemoradiotherapy in locally advanced non-small-cell lung cancer: a post-hoc analysis of the PACIFIC trial. Lancet Oncol. 2026 Aug;27(8):1043-1056. doi: 10.1016/S1470-2045(26)00191-9. Epub 2026 Jul 3.

    PubMed 42398520
  • Naidoo J, Antonia S, Wu YL, Cho BC, Thiyagarajah P, Mann H, Newton M, Faivre-Finn C. Brief Report: Durvalumab After Chemoradiotherapy in Unresectable Stage III EGFR-Mutant NSCLC: A Post Hoc Subgroup Analysis From PACIFIC. J Thorac Oncol. 2023 May;18(5):657-663. doi: 10.1016/j.jtho.2023.02.009. Epub 2023 Feb 24.

    PubMed 36841540
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Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing MEDI4736 in people with Non-Small Cell Lung Cancer, run by AstraZeneca at 236 sites in 26 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 5 inclusion and 6 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 10 Oct 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 236 sites in United States, Japan, Spain, France, Australia and 21 more countries. 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. Some participants in this study may receive a placebo. 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 30 Jan 2019). 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?

Progression Free Survival Based on Blinded Independent Central Review (BICR) According to Response Evaluation Criteria in Solid Tumors (RECIST 1.1) (time frame: Tumor scans performed at baseline then every ~8 weeks up to 48 weeks, then every ~12 weeks thereafter until confirmed disease progression. Assessed until 13 Feb 2017 DCO; up to a maximum of approximately 3 years.). The study lists 2 primary outcomes in all. 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 NCT02125461, which also lists 16 linked publications.

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 10 Oct 2023.

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