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pemetrexed

Generic: PEMETREXED DISODIUM·Brand: ALIMTA, Alimta, PEMETREXED, PEMETREXED DISODIUM, PEMFEXY, Pemfexy

pemetrexed: sourced relationships with 1 company · 139 clinical trials tracked · 2 FDA decisions.

pemetrexed evidence translation

What we can confirm

2 FDA records · 139 tracked trials

What it means

Source-backed records connect pemetrexed to RDY; that link alone does not prove the drug works.

What to watch

Watch active trials and any change in FDA or trial status.
BioSniper AIPage evidence connected

Prepared research question

How could pemetrexed → RDY affect its developer, and what evidence supports the link?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence8 indications · 19 study sponsors
Dated Pipeline Records (1)
CompanyDated record stage
DR REDDYS LABORATORIES LTD (RDY)
Reported 2020-05-14 · Current development: unknownSource
Approved
Clinical Trial Registry Records (139)showing 10 most recent

A Randomized, Double-Blind, Multicenter, Phase II/III Study to Evaluate HLX37 (Recombinant Human Anti-PD-L1 and Anti-VEGF Bispecific Antibody) in Combination With Chemotherapy Versus Pembrolizumab in Combination With Chemotherapy for First-Line Therapy of Advanced Non-Small Cell Lung Cancer

NCT07865910Registry updated 2026-10-08·Phase 2/Phase 3
Not yet recruiting

Primary endpoint: PFS assessed by BICR (Phase2&3)

InterventionalRandomizedtriple1,438 targetStarted 2026-11Completion 2031-1216 sites · ChinaShanghai Henlius Biotech

A Randomized Phase II Study Evaluating Upfront SRT to All Brain Metastases Followed by Ivonescimab Plus Chemotherapy Versus Upfront Ivonescimab Plus Chemotherapy in Patients With Asymptomatic Active Brain Metastases From NSCLC

NCT07234877Registry updated 2026-06-04·Phase 2
Not yet recruiting

Primary endpoint: Intracranial progression-free survival based on local assessment using RANO-BM criteria

InterventionalRandomizedopen158 targetStarted 2026-11Completion 2032-0426 sites · Austria, France, Germany, Greece…European Organisation for Research and Treatment of Cancer - EORTC

A Phase 2, Open-label Clinical Study to Evaluate the Safety and Efficacy of MK-2010 as Monotherapy and in Combination

NCT07793942Registry updated 2026-10-08·Phase 2
Not yet recruiting

Primary endpoint: Number of Participants with Adverse Events (AEs)

Interventionalopen480 targetStarted 2026-10Completion 2030-076 sites · Switzerland, United StatesMerck Sharp & Dohme LLC

Phase I Pilot Trial of Golcadomide With Pemetrexed, Rituximab, and Dexamethasone for Relapsed and Refractory CNS Lymphomas

NCT07608731Registry updated 2026-08-21·Phase 1
Not yet recruiting

Primary endpoint: Safety of Golcadomide + Pemetrexed, Rituximab and Dexamethasone

Interventionalopen18 targetStarted 2026-10Completion 2029-091 site · United StatesAllison Winter

A Phase III, Randomized, Open-label Study of Izalontamab Brengitecan (BMS-986507) in Combination With Osimertinib Versus Osimertinib Monotherapy or Osimertinib in Combination With Platinum-based Chemotherapy as First-Line Therapy in Patients With EGFR-Mutant Locally Advanced or Metastatic Non-small Cell Lung Cancer

NCT07680790Registry updated 2026-08-24·Phase 3·BMY
Not yet recruiting

Primary endpoint: Progression-Free Survival (PFS) using blinded independent central review (BICR) assessment as defined by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1)

InterventionalRandomizedopen850 targetStarted 2026-09Completion 2031-1250 sites · Argentina, Australia, Brazil, United StatesBristol-Myers Squibb

A Phase 2, Randomized, Open-label, Study Assessing the Safety, Tolerability and Efficacy of Imzokitug in Combination With Pumitamig and Platinum-Doublet Chemotherapy (PDCT) Versus Pumitamig and PDCT as First-line Treatment for Participants With Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC)

NCT07680764Registry updated 2026-10-02·Phase 2·BMY
Recruiting

Primary endpoint: Objective response rate (ORR) by investigator (per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1)

InterventionalRandomizedopen160 targetStarted 2026-09Completion 2030-0973 sites · Argentina, Australia, Brazil, Chile…Bristol-Myers Squibb

A Prospective, Single-arm, Multicenter Phase II Clinical Study to Evaluate the Efficacy and Safety of Spatially Fractionated Radiotherapy Combined With Tislelizumab and Platinum-based Doublet Chemotherapy as Induction/Conversion Therapy for Potentially Resectable Stage III Non-small Cell Lung Cancer With Bulky Disease.

NCT07775040Registry updated 2026-08-20·Phase 2
Not yet recruiting

Primary endpoint: Major Pathological Response (MPR) Rate

Interventionalopen43 targetStarted 2026-08Completion 2030-061 site · ChinaSichuan Cancer Hospital and Research Institute

A Phase 2 Study Evaluating the Safety and Efficacy of Neoadjuvant Amivantamab in Combination With Lazertinib or Chemotherapy in Resectable EGFR-Mutated Non-Small Cell Lung Cancer

NCT07586202Registry updated 2026-09-25·Phase 2
Recruiting

Primary endpoint: Major Pathologic response (MPR)

Interventionalopen68 targetStarted 2026-07Completion 2028-0423 sites · Canada, China, South Korea, Spain…Janssen Research & Development, LLC

A Phase 2 Open-Label, Multi-Center Study of BMS-986504 as Monotherapy and in Combination With Other Agents in Participants With Advanced and/or Metastatic Solid Tumors With Homozygous MTAP Deletion

NCT07492680Registry updated 2026-10-06·Phase 2·BMY
Recruiting

Primary endpoint: Part 1: Number of participants who achieve Objective Response (OR)

Interventionalopen260 targetStarted 2026-07Completion 2032-0558 sites · Belgium, Canada, China, France…Bristol-Myers Squibb

Phase 3, Randomized, Open-Label Study of Nogapendekin Alfa Inbakicept in Combination With Standard of Care Versus Standard of Care as First-Line Treatment for Patients With Advanced or Metastatic Non-Small Cell Lung Cancer

NCT07524257Registry updated 2026-06-22·Phase 3·IBRX
Withdrawn

Primary endpoint: Progression-Free Survival (PFS) by BICR (RECIST v1.1)

InterventionalRandomizedopen0 targetStarted 2026-05Completion 2029-12ImmunityBio, Inc.
FDA Decisions2 records
Approval(RDY)FDA ↗
ANDA202596UNKNOWNIntravenousPowder
Tentative Approval(RDY)FDA ↗
NDA208297Type 5 - New Formulation or New ManufacturerStandardOtherInjectable

Frequently asked questions

Which companies have sourced relationships with pemetrexed?

pemetrexed has dated SEC/FDA relationship records for DR REDDYS LABORATORIES LTD.

How many clinical trials involve pemetrexed?

BioSniper tracks 139 clinical trials involving pemetrexed.

What is pemetrexed's latest FDA decision?

The most recent tracked FDA decision for pemetrexed is Approval, dated May 25, 2022.