Traws Pharma

25 total trials 22 completed

Traws Pharma sponsors 25 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 22 completed. 4 of these trials are in Phase 3-4 (later-stage) and 21 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Myelodysplastic Syndrome, with 3 trials.

Trial Pipeline

25 total, page 1 of 1

TERMINATED Phase 3

Controlled Study of Rigosertib Versus Physician's Choice of Treatment in MDS Patients After Failure of an HMA

NCT02562443

TERMINATED Phase 1

Dose-escalation, Safety and Pharmacokinetic Study of Briciclib in Advanced Solid Tumors

NCT02168725

COMPLETED Phase 1

Metabolism and Excretion of [14C]-Rigosertib After Infusion to Volunteers

NCT02030639

COMPLETED Phase 1

Platinum-based Chemoradiotherapy and Rigosertib in Head and Neck Cancer

NCT02107235

COMPLETED Phase 1

Phase II Part 2 Expansion of Oral Rigosertib in Combination With Azacitidine

NCT01926587

COMPLETED Phase 3

Efficacy and Safety of IV Rigosertib in MDS Patients With Excess Blasts Progressing After Azacitidine or Decitabine

NCT01928537

COMPLETED Phase 2

Oral Rigosertib in Low Risk MDS Patients Refractory to ESAs

NCT01904682

COMPLETED Phase 2

Oral Rigosertib for Squamous Cell Carcinoma

NCT01807546

COMPLETED Phase 2

Efficacy and Safety of Oral Rigosertib in Transfusion-dependent, Low or Int-1 or Trisomy 8 Int-2 Myelodysplastic Syndrome

NCT01584531

COMPLETED Phase 3

Gemcitabine and ON 01910.Na in Previously Untreated Metastatic Pancreatic Cancer

NCT01360853

COMPLETED Phase 3

Randomized Study of ON 01910.Na in Refractory Myelodysplastic Syndrome Patients With Excess Blasts

NCT01241500

COMPLETED Phase 1

Safety, Pharmacokinetics and Clinical Activity of Oral Rigosertib in Solid Tumors

NCT01168011

COMPLETED Phase 1

Safety and Efficacy of 72-hour and 120-hour Infusion of Rigosertib in Acute Myeloid Leukemia (AML) and Acute Lymphoid Leukemia (ALL)

NCT01167166

COMPLETED Phase 1

Safety of 24-hour Infusion of ON 01910.Na in Combination With Gemcitabine in Advanced Solid Tumors

NCT01165905

COMPLETED Phase 1

Safety and Pharmacokinetic Study of Oral ON 01910.Na in Patients With Myelodysplastic Syndrome

NCT01048619

TERMINATED Phase 1

Safety Study of ON 013105 in Lymphoma and Acute Lymphoid Leukemia

NCT01049113

COMPLETED Phase 2

Efficacy and Safety of ON 01910.Na in Myelodysplastic Syndrome (MDS) Patients With Trisomy 8 or Classified as Intermediate-1, -2 or High Risk

NCT00906334

COMPLETED Phase 2

Effect of 2-h Infusion of ON 01910.Na in Ovarian Cancer Patients

NCT00856791

COMPLETED Phase 1

Study of 72-Hour Infusion of ON 01910.Na in Patients With MDS or AML

NCT00854945

COMPLETED Phase 1

Dose Escalation Study of Gemcitabine and ON 01910.Na in Solid Tumors

NCT01125891

COMPLETED Phase 1

Phase I Study of ON 01910.Na in Refractory Leukemia or Myelodysplastic Syndrome (MDS)

NCT00854646

COMPLETED Phase 1

Safety of ON 01910.Na and Irinotecan or ON 01910.Na and Oxaliplatin in Patients With Hepatoma

NCT00861783

COMPLETED Phase 1

Safety Study of ON 01910.Na in Combination With Irinotecan or Oxaliplatin

NCT00861328

COMPLETED Phase 1

Safety of ON 01910.Na as a 3-day Infusion in Patients With Advanced Cancer

NCT01538537

COMPLETED Phase 1

Safety of 24-Hour Infusion of ON 01910.Na in Patients With Advanced Cancer

NCT01538563

Phase Distribution

PhaseTrial count
Phase 1 16
Phase 2 5
Phase 3 4

What the Pipeline for Traws Pharma Shows

According to the ClinicalTrials.gov registry, Traws Pharma is linked to 25 US clinical trials across every stage of research activity. Of those, 0 studies are currently recruiting, about 0% of the sponsor's indexed portfolio, and 22 are already marked complete, representing roughly 88% of the total.

The phase mix for Traws Pharma reports 4 late-stage studies (Phase 3 and Phase 4 combined) and 21 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Traws Pharma is Myelodysplastic Syndrome with 3 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.