PharmaMar

32 total trials 4 currently recruiting 20 completed

PharmaMar sponsors 32 registered US clinical trials on ClinicalTrials.gov, 4 of them currently recruiting, and 20 completed. 5 of these trials are in Phase 3-4 (later-stage) and 27 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Advanced Solid Tumors, with 2 trials.

Trial Pipeline

32 total, page 1 of 1

RECRUITING Phase 1

Study of PM54 in Combination With Immunotherapy in Adult Participants With Advanced Malignancies

NCT07644039

RECRUITING Phase 3

Study of Lurbinectedin in Combination With Doxorubicin Versus Doxorubicin Alone as First-line Treatment in Participants With Metastatic Leiomyosarcoma (SaLuDo)

NCT06088290

RECRUITING Phase 1

Clinical Trial of PM54 in Advanced Solid Tumors Patients.

NCT05841563

RECRUITING Phase 1

PM14 Administered Intravenously to Patients with Advanced Solid Tumors

NCT05076396

ACTIVE NOT RECRUITING Phase 3

Clinical Trial of Lurbinectedin as Single-agent or in Combination With Irinotecan Versus Topotecan or Irinotecan in Patients With Relapsed Small-cell Lung Cancer (LAGOON)

NCT05153239

COMPLETED Phase 2

Clinical Trial of PM60184 in Advanced Colorectal Cancer After Standard Treatment

NCT03427268

TERMINATED Phase 2

A Study of Plitidepsin in Patients With Relapsed or Refractory Angioimmunoblastic T-cell Lymphoma

NCT03070964

COMPLETED Phase 3

Clinical Trial of Lurbinectedin (PM01183)/Doxorubicin Versus CAV or Topotecan as Treatment in Patients With Small-Cell Lung Cancer

NCT02566993

COMPLETED Phase 1

Pharmacokinetic Study of Lurbinectedin in Combination With Irinotecan in Patients With Selected Solid Tumors

NCT02611024

COMPLETED Phase 2

Clinical Trial of Lurbinectedin (PM01183) in Selected Advanced Solid Tumors

NCT02454972

COMPLETED Phase 2

Evaluation of the Effect of Lurbinectedin (PM01183) on Cardiac Repolarization in Patients With Selected Solid Tumors

NCT02451007

COMPLETED Phase 3

Clinical Trial of Lurbinectedin (PM01183) in Platinum Resistant Ovarian Cancer Patients

NCT02421588

COMPLETED Phase 1

Multicenter, Open-label, Clinical and Pharmacokinetic Study of PM060184 in Combination With Gemcitabine in Selected Patients With Advanced Solid Tumors

NCT02533674

COMPLETED Phase 2

A Clinical Study in Three-arm of Lurbinectedin (PM01183) Alone or in Combination With Gemcitabine and a Control Arm With Docetaxel as Second Line Treatment in Non-Small Cell Lung Cancer (NSCLC) Patients

NCT01951157

COMPLETED Phase 1

Phase I Study of Lurbinectedin (PM01183) in Combination With Paclitaxel, With or Without Bevacizumab, in Selected Advanced Solid Tumors

NCT01831089

COMPLETED Phase 2

A Phase II Clinical Trial of PM01183 in BRCA 1/2-Associated or Unselected Metastatic Breast Cancer

NCT01525589

COMPLETED Phase 1

Study of PM01183 in Non-Colorectal Cancer Patients as a Days 1 and 8 Intravenous Short Infusion Every 3 Weeks

NCT01405391

COMPLETED Phase 1

Clinical Study of PM01183 in Patients With Acute Leukemia or Relapsed/Refractory Myelodysplastic Syndrome

NCT01314599

COMPLETED Phase 1

Study of PM060184 in Patients With Advanced Solid Tumors

NCT01299636

COMPLETED Phase 2

Study of Zalypsis® (PM00104) in Patients With Unresectable Locally Advanced and/or Metastatic Ewing Family of Tumors (EFT) Progressing After at Least One Prior Line of Chemotherapy

NCT01222767

COMPLETED Phase 2

Clinical Trial of Aplidin® in Patients With Primary Myelofibrosis

NCT01149681

COMPLETED Phase 3

Aplidin - Dexamethasone in Relapsed/Refractory Myeloma

NCT01102426

TERMINATED Phase 2

Clinical Trial of PM00104 (Zalypsis®) in Patients With Advanced and/or Metastatic Endometrial or Cervical Cancer Previously Treated With One Line of Systemic Chemotherapy

NCT00900562

COMPLETED Phase 1

Phase I, Multicenter, Open-label, Dose-escalating, Clinical and Pharmacokinetic Study of PM01183 in Patients With Advanced Solid Tumors

NCT00877474

COMPLETED Phase 1

Trial of PM02734 Administered in Combination With Erlotinib in Patients With Advanced Malignant Solid Tumors

NCT00884845

COMPLETED Phase 1

Study of Plitidepsin in Combination With Sorafenib or Gemcitabine in Patients With Advanced Solid Tumors or Lymphomas

NCT00788099

TERMINATED Phase 1

Clinical Study of Plitidepsin (Aplidin®) in Combination With Cytarabine in Patients With Relapsed/Refractory Leukemia

NCT00780143

TERMINATED Phase 1

A Phase I Study of Zalypsis (PM00104) in Subjects With Advanced Malignant Solid Tumors or Lymphoma

NCT00359294

TERMINATED Phase 1

A Phase I Study of PM02734 in Subjects With Advanced Malignant Solid Tumors

NCT00404521

COMPLETED Phase 2

A Study of Aplidin (Plitidepsin) 3 h iv in Subjects With Relapsing or Refractory Multiple Myeloma

NCT00229203

TERMINATED Phase 2

A Study of Aplidin ( Plitidepsin) in Subjects With Advanced Prostate Cancer

NCT00780975

TERMINATED Phase 2

Ecteinascidin 743 in Treating Patients With Malignant Mesothelioma

NCT00027508

What the Pipeline for PharmaMar Shows

According to the ClinicalTrials.gov registry, PharmaMar is linked to 32 US clinical trials across every stage of research activity. Of those, 4 studies are currently recruiting, about 13% of the sponsor's indexed portfolio, and 20 are already marked complete, representing roughly 63% of the total.

The phase mix for PharmaMar reports 5 late-stage studies (Phase 3 and Phase 4 combined) and 27 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for PharmaMar is Advanced Solid Tumors with 2 linked trials, and 6 other condition areas appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.