Alimta® (pemetrexed)
Consistent with the company's policy of public data disclosure, this clinical trial results section includes result summaries of completed Lilly-sponsored clinical studies conducted on Lilly marketed products since July 1, 2004. The results of all Phase I, II, and III trials conducted in support of a product’s initial registration will be disclosed regardless of outcome, no later than when the first indication is approved and the drug is commercially available for patient use anywhere in the world. The results of all subsequent Phase II, III, and IV trials conducted after initial approval will be similarly disclosed within one year of trial completion. A trial’s results, irrespective of study phase, will be disclosed as soon as possible if there are significant safety findings.
Consistent with ICH E3 guidelines, Lilly will disclose the results of primary and secondary outcome measures that are specified in the study protocol, as well as additional safety and efficacy results that impact patient care and the use of our products. Also, Lilly discloses a comprehensive description of the trial design and methodology for each study. Results will be disclosed regardless of whether they support the hypothesis being tested or are contrary to the predicted outcome. Clinical trial results will be publicly disclosed as stated above, unless posting would compromise publication in a peer reviewed medical journal or contravene national laws or regulations. Results of studies that are under review by peer-reviewed journals that prohibit pre-publication disclosure will be posted on the registry at the time of publication. Clinical trial results are also disclosed through presentations and abstract submissions at professional scientific meetings.
The registry is also populated with the results of core efficacy and safety registration trials for products first approved after July 1, 1994.
Included are trial result summaries that are completed to date. The company will continue to disclose additional summaries and publication citations as they become available.
Summaries of clinical study results are intended to report the results of the study that were known at the time of each study's completion. The information contained in these summaries is not intended to promote or otherwise commercialize (directly or indirectly) any off-label or unapproved uses of Lilly medicines, nor is it intended to provide a comprehensive analysis of all data currently available regarding a particular drug. In some cases, more current information regarding a drug, including post-hoc analyses and meta-analyses, may be available as part of the general body of scientific knowledge in forms such as manuscripts, abstracts, or posters.
Clinical studies on Lilly products may also be sponsored and reported by
parties other than Lilly
in other clinical trial registries.
Trial Results
The following trials have been conducted for Alimta.
| Disease |
Trial ID |
Trial Title |
Trial
Phase |
Adenocarcinoma
|
9508 |
Phase II Study of Gemcitabine and Pemetrexed in Primary Unknown Adenocarcinoma
|
2 |
Bladder Cancer |
4698 |
A Phase 2 Study of ALIMTA (Pemetrexed) in Patients with Advanced or Metastatic Recurrent Transitional Cell Carcinoma of the Urothelium
|
2 |
Bladder Cancer |
4699 |
A Phase 2 Trial of ALIMTA® Plus Gemcitabine in Locally Advanced or Metastatic Transitional Cell Carcinoma of the Urothelium
|
2 |
Bladder Cancer |
8279 |
Phase II Trial of Pemetrexed Disodium and Gemcitabine in Advanced Urothelial Cancer
|
2 |
Breast Cancer |
4028 |
A Phase 1/2 Dose-Escalating Study of ALIMTA (pemetrexed) and Epirubicin Administered Every 21 Days in Patients with Locally Advanced or Metastatic Breast Cancer
|
1 / 2 |
Breast Cancer |
2245 |
A Phase II Study of a Combination of Pemetrexed and Gemcitabine in Patients with Metastatic Breast Cancer: an NCCTG Study
|
2 |
Breast Cancer |
7491 |
A Randomized, Double-Blind, Phase 2 Study of Two Doses of ALIMTA® as First-Line Chemotherapy for Advanced Breast Cancer
|
2 |
Breast Cancer |
7771 |
A Phase 2 Study of ALIMTA and Carboplatin in the Treatment of Patients with Locally Advanced or Metastatic Breast Cancer
|
2 |
Breast Cancer |
9305 |
A Phase 2 Study of Biweekly Pemetrexed and Gemcitabine in Patients with Metastatic Breast Cancer
|
2 |
Cervical Cancer |
8367 |
A Phase II Evaluation of Pemetrexed In the Treatment of Recurrent Carcinoma of the Cervix
|
2 |
Colorectal Cancer
|
2927 |
A Phase 1/2 Trial of Pemetrexed Plus Irinotecan Administered Every 21 Days in Patients with Previously Treated Locally Advanced or Metastatic Colorectal Cancer
|
1 / 2 |
Colorectal Cancer
|
2929 |
A Randomized Phase 2 Trial of Alimta plus Irinotecan versus Leucovorin-Modulated
Fluorouracil plus Irinotecan in First-Line Treatment of Locally Advanced or Metastatic Colorectal Cancer
|
2 |
Colorectal Cancer |
5142 |
Phase II Trial Of ALIMTA (LY231514, Pemetrexed) Plus Oxaliplatin Administered Every 21 Days For First-Line Treatment Of Patients With Advanced Colorectal Cancer.
|
2 |
Gastric Cancer |
6154 |
Open-Label Single-Arm Phase 2 Study of ALIMTA plus Cisplatin in Korean Patients with Advanced Gastric Carcinoma
|
2 |
Gastric Cancer |
8059 |
Pemetrexed Plus Oxaliplatin in the Management of Advanced Gastric Cancer: A Multicenter Phase II Trial
|
2 |
Liver Cancer |
9417 |
Single-Agent Pemetrexed in Patients with Advanced or Metastatic Hepatoma
|
2 |
Malignant Pleural Mesothelioma |
1307 |
Phase I trial of Alimta® (pemetrexed) and cisplatin every 21 days in patients with locally advanced or metastatic solid tumors
|
1 |
Malignant Pleural Mesothelioma |
1806 |
A Phase 1 Pharmacokinetic Trial of Alimta® (pemetrexed) Administered Intravenously Every 3 Weeks in Advanced Cancer Patients with Varying Degrees of Renal Function
|
1 |
Malignant Pleural Mesothelioma |
2234 |
A Phase 1 Clinical Trial of Alimta® (pemetrexed) in Combination with Carboplatin in Patients with Malignant Pleural Mesothelioma
|
1 |
Malignant Pleural Mesothelioma |
5249 |
Phase I/II Study of LY231514 and Cisplatin Combination Therapy in Patients with Malignant Pleural Mesothelioma
|
1 / 2 |
Malignant Pleural Mesothelioma |
3653 |
A Phase 2 Trial of LY231514 Administered Intravenously Every 21 Days in Patients with Malignant Pleural Mesothelioma |
2 |
Malignant Pleural Mesothelioma |
7214 |
Pemetrexed Plus Gemcitabine as Front-line Chemotherapy for Patients with Malignant Pleural or Peritoneal Mesothelioma: A Phase II Clinical Trial |
2 |
Malignant Pleural Mesothelioma |
10512 |
Safety Confirmation Study of LY231514 Plus Cisplatin in Patients With Malignant Pleural Mesothelioma |
2 |
Malignant Pleural Mesothelioma |
2258 |
A Single-blind Randomized Phase 3 Trial of Alimta® (pemetrexed) plus Cisplatin versus Cisplatin Alone in Patients with Malignant Pleural Mesothelioma |
3 |
Malignant Pleural Mesothelioma |
5362 |
A Randomized Phase 3 Trial Comparing ALIMTA Plus Best Supportive Care versus
Best Supportive Care Alone in Previously Treated Patients with Locally Advanced or Metastatic
Malignant Pleural Mesothelioma |
3 |
Metastatic Cancer |
7058 |
A Phase 1 Dose-Escalating Study of Pemetrexed in Combination with Gemcitabine and Cisplatin in Patients with Locally Advanced or Metastatic Cancer |
1 |
Non-Small Cell Lung Cancer (NSCLC), 1st Line |
1809 |
A Phase 1/2 Dose-Escalating Study Of LY231514 and Vinorelbine Administered Every 21 Days In Patients With Locally Advanced Or Metastatic Cancer
|
1 / 2 |
Non-Small Cell Lung Cancer (NSCLC), 1st Line |
7221 |
Phase 1/2 Dose-Escalating Study of Biweekly Pemetrexed and Gemcitabine in Patients with Advanced Cancer
|
1 / 2 |
Non-Small Cell Lung Cancer (NSCLC), 1st Line |
5114 |
Alimta Plus Carboplatin Or Alimta Plus Oxaliplatin As Front-Line Chemotherapy For Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer: A Randomized Phase 2 Clinical Trial
|
2 |
Non-Small Cell Lung Cancer (NSCLC), 1st Line |
5115 |
A Phase II Clinical Trial Evaluating Three Schedules of ALIMTA® Plus Gemcitabine as Front-Line Chemotherapy for Patients With Locally Advanced or Metastatic Non-Small Cell Lung Cancer |
2 |
Non-Small Cell Lung Cancer (NSCLC), 1st Line |
5119 |
A Multicenter Phase 2 Randomized Trial of Single-Agent ALIMTA® or ALIMTA with Sequentially Administered GEMZAR® as First-Line Chemotherapy in Elderly Patients or Patients who are not Eligible for Platinum-Based Chemotherapy with Advanced NSCLC. |
2 |
Non-Small Cell Lung Cancer (NSCLC), 1st Line |
6142 |
Alimta Plus Carboplatin as Front-Line Chemotherapy for Patients With Locally Advanced or Metastatic Non-Small Cell Lung Cancer: A Phase II Clinical Trial
|
2 |
Non-Small Cell Lung Cancer (NSCLC), 1st Line |
7211 |
Alimta Plus Gemcitabine as Front-Line Chemotherapy for Patients with Locally Advanced or Metastatic Non-Small Cell Lung Cancer: A Phase II Clinical Trial
|
2 |
Non-Small Cell Lung Cancer (NSCLC), 1st Line |
7213 |
ALIMTA Plus Gemcitabine as Front-line Chemotherapy for Patients with Locally
Advanced or Metastatic Non-Small-Cell Lung Cancer: A Phase II Clinical Trial
|
2 |
Non-Small Cell Lung Cancer (NSCLC), 1st Line |
2938 |
A Randomized Phase 3 Trial of ALIMTA® and Cisplatin versus GEMZAR® and Cisplatin in Patients with Locally Advanced or Metastatic Non-Small Cell Lung Cancer
|
3 |
Non-Small Cell Lung Cancer (NSCLC), 2nd Line |
1292 |
A Phase 1 Study of Alimta® (pemetrexed) using a daily x 5 q 21 schedule
|
1 |
Non-Small Cell Lung Cancer (NSCLC), 2nd Line |
1293 |
A Phase 1 Study of Alimta® (pemetrexed) Administered as a Bolus Infusion Every 21 Days
|
1 |
Non-Small Cell Lung Cancer (NSCLC), 2nd Line |
1294 |
A Phase 1 Study of Alimta® (pemetrexed) Administered as a Bolus Given Intravenously Every 7 Days
|
1 |
Non-Small Cell Lung Cancer (NSCLC), 2nd Line |
1790 |
A Phase 2 Trial of Alimta® (pemetrexed) Administered Intravenously Every 21 Days in Patients with Non-Small Cell Lung Cancer Who Have Failed Previous Chemotherapy
|
2 |
Non-Small Cell Lung Cancer (NSCLC), 2nd Line |
6685 |
Open-Label Single-Arm Phase 2 Study of ALIMTA in Patients with Advanced Non-Small Cell Lung Cancer Who Have Had Prior Chemotherapy
|
2 |
Non-Small Cell Lung Cancer (NSCLC), 2nd Line |
4881 |
A Phase 3 Trial of Alimta® (Pemetrexed) vs Docetaxel in Patients with Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) Who Were Previously Treated with Chemotherapy
|
3 |
Non-Small Cell Lung Cancer (NSCLC), 2nd Line |
8433 |
A Randomized Phase 3 Study of Two Doses of Alimta in Patients with Locally Advanced or Metastatic Non-Small Cell Lung Cancer Who Have Failed a Prior Platinum-Containing Chemotherapy
|
3 |
Ovarian Cancer |
8408 |
Phase 1 Dose-Escalating Study of ALIMTA® (pemetrexed) and GEMZAR® (gemcitabine) Given Every 14 Days in Patients with an Advanced Malignancy or Ovarian Cancer
|
1 |
Ovarian Cancer |
7127 |
Phase II Trial Evaluating GEMZAR® and ALIMTA® in the Treatment of Patients with Recurrent Platinum-Sensitive or Platinum-Resistant Epithelial Ovarian or Primary Peritoneal Cancer Undergoing Second-Line Chemotherapy
|
2 |
Ovarian Cancer |
9710 |
A Randomized, Double-Blind, Phase 2 Study of Two Doses of Pemetrexed in the
Treatment of Platinum-Resistant, Epithelial Ovarian or Primary Peritoneal Cancer
|
2 |
Pancreatic Cancer |
8621 |
A Phase 2 Trial of Pemetrexed (ALIMTA®) in Pretreated Patients with Unresectable or Metastatic Cancer of the Pancreas |
2 |
Pancreatic Cancer |
5148 |
A Phase 3 Trial of ALIMTA Plus GEMZAR Versus GEMZAR in Patients With Unresectable or Metastatic Cancer of the Pancreas |
3 |
Prostate Cancer |
9772 |
Phase 1/2 Trial of ALIMTA in Androgen-Independent Metastatic and/or Unresectable Prostate Cancer |
1 / 2 |
Small Cell Lung Cancer |
7209 |
Phase II Trial of ALIMTA in Relapsed Small Cell Lung Cancer |
2 |
Small Cell Lung Cancer
|
7210 |
A Randomized Phase II Trial of ALIMTA/Cisplatin and ALIMTA/Carboplatin in Extensive Stage Small Cell Lung Cancer
|
2 |
Solid Tumors
|
6147 |
A Phase 1 Study of Pemetrexed (LY231514, Alimta) in Children and Adolescents with Recurrent Solid Tumors
|
1 |
Solid Tumors
|
8366 |
A Phase II Trial of Pemetrexed (Alimta®, LY231514, IND #40061) in the Treatment of Recurrent or Persistent Low Risk Gestational Trophoblastic Tumor
|
2 |
|