Traws Pharma
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
Controlled Study of Rigosertib Versus Physician's Choice of Treatment in MDS Patients After Failure of an HMA
NCT02562443
Dose-escalation, Safety and Pharmacokinetic Study of Briciclib in Advanced Solid Tumors
NCT02168725
Metabolism and Excretion of [14C]-Rigosertib After Infusion to Volunteers
NCT02030639
Platinum-based Chemoradiotherapy and Rigosertib in Head and Neck Cancer
NCT02107235
Phase II Part 2 Expansion of Oral Rigosertib in Combination With Azacitidine
NCT01926587
Efficacy and Safety of IV Rigosertib in MDS Patients With Excess Blasts Progressing After Azacitidine or Decitabine
NCT01928537
Oral Rigosertib in Low Risk MDS Patients Refractory to ESAs
NCT01904682
Oral Rigosertib for Squamous Cell Carcinoma
NCT01807546
Efficacy and Safety of Oral Rigosertib in Transfusion-dependent, Low or Int-1 or Trisomy 8 Int-2 Myelodysplastic Syndrome
NCT01584531
Gemcitabine and ON 01910.Na in Previously Untreated Metastatic Pancreatic Cancer
NCT01360853
Randomized Study of ON 01910.Na in Refractory Myelodysplastic Syndrome Patients With Excess Blasts
NCT01241500
Safety, Pharmacokinetics and Clinical Activity of Oral Rigosertib in Solid Tumors
NCT01168011
Safety and Efficacy of 72-hour and 120-hour Infusion of Rigosertib in Acute Myeloid Leukemia (AML) and Acute Lymphoid Leukemia (ALL)
NCT01167166
Safety of 24-hour Infusion of ON 01910.Na in Combination With Gemcitabine in Advanced Solid Tumors
NCT01165905
Safety and Pharmacokinetic Study of Oral ON 01910.Na in Patients With Myelodysplastic Syndrome
NCT01048619
Safety Study of ON 013105 in Lymphoma and Acute Lymphoid Leukemia
NCT01049113
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
Effect of 2-h Infusion of ON 01910.Na in Ovarian Cancer Patients
NCT00856791
Study of 72-Hour Infusion of ON 01910.Na in Patients With MDS or AML
NCT00854945
Dose Escalation Study of Gemcitabine and ON 01910.Na in Solid Tumors
NCT01125891
Phase I Study of ON 01910.Na in Refractory Leukemia or Myelodysplastic Syndrome (MDS)
NCT00854646
Safety of ON 01910.Na and Irinotecan or ON 01910.Na and Oxaliplatin in Patients With Hepatoma
NCT00861783
Safety Study of ON 01910.Na in Combination With Irinotecan or Oxaliplatin
NCT00861328
Safety of ON 01910.Na as a 3-day Infusion in Patients With Advanced Cancer
NCT01538537
Safety of 24-Hour Infusion of ON 01910.Na in Patients With Advanced Cancer
NCT01538563
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 16 |
| Phase 2 | 5 |
| Phase 3 | 4 |
Therapeutic Areas
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.
Read our methodology - how this data is sourced, computed, and verified.
Related
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.