Whitehawk Therapeutics, Inc. (WHWK)
Whitehawk Therapeutics, Inc., a clinical-stage oncology therapeutics company that develops technologies to establish tumor biology for cancer treatments. It provides three next generation antibody drug conjugates (ADC) portfolio to treat cancer. The company was formerly known as Aadi Bioscience, Inc. and changed its name to Whitehawk Therapeutics, Inc. in August 2021. Whitehawk Therapeutics, Inc. was incorporated in 2007 and is headquartered in Morristown, New Jersey.
Sector: Pharmaceutical Preparations
Industry: Biotechnology
Whitehawk Therapeutics Inc
Trials need funding. See this company's dilution risk and cash position.
- Phase 2Completed
The TIME-2 Study: A Phase 2 Study of AKB-9778, a Novel Tie-2 Activator, in Patients With Diabetic Macular Edema
AKB-9778, ranibizumab
Diabetic Macular Edema (DME)
NCT02050828Enrollment144StartJan 2014Primary CompletionApr 2015CompletionMay 2015 - Phase 2Completed
Open Label Study to Assess the Efficacy and Safety of AKB-9778 in Subjects With Macular Edema Due to RVO
AKB-9778
Retinal Vein Occlusion
NCT02387788Enrollment16StartJan 2015Primary CompletionApr 2017CompletionApr 2017 - Phase 2Completed
A Phase 2 Study of Nab-sirolimus (ABI-009) in Patients With Advanced Malignant PEComa
nab-Sirolimus
Malignant PEComa
NCT02494570Enrollment34StartOct 2015Primary CompletionNov 2021CompletionApr 2022 - Phase 2Completed
Nab-sirolimus in Recurrent High Grade Glioma and Newly Diagnosed Glioblastoma
nab-sirolimus, nab-sirolimus + temozolomide
High Grade Recurrent Glioma and Newly Diagnosed Glioblastoma
NCT03463265Enrollment62StartAug 2018Primary CompletionAug 2022CompletionAug 2022 - Phase 2Withdrawn
ABI-009 (Nab-sirolimus) in Patients With Genetically-confirmed Leigh or Leigh-like Syndrome
ABI-009
Leigh Syndrome
NCT03747328Enrollment0StartApr 2022est.Primary CompletionDec 2024est.CompletionMar 2025est. - Phase 2Completed
Phase 2 Basket Trial of Nab-sirolimus in Patients With Malignant Solid Tumors With Pathogenic Alterations in TSC1/TSC2 Genes (PRECISION 1)
nab-sirolimus
Tumor, Tumor, Solid +19
NCT05103358Enrollment128StartMar 2022Primary CompletionDec 2024CompletionDec 2024 - Phase 2Recruiting
Trial of Nab-Sirolimus in Combination With Letrozole in Patients With Advanced or Recurrent Endometrioid Endometrial Cancer
nab-sirolimus
Endometrial Cancer, Endometrioid Tumor +4
NCT05997017Enrollment29StartDec 2023Primary CompletionDec 2026est.CompletionJun 2027est. - Phase 2Completed
Trial of Nab-sirolimus in Patients With Well-differentiated Neuroendocrine Tumors (NETs) of the Gastrointestinal Tract, Lung, or Pancreas Who Have Not Received Prior Treatment With mTOR Inhibitors
nab-sirolimus
Neuroendocrine Tumors, NET +3
NCT05997056Enrollment12StartOct 2023Primary CompletionOct 2025CompletionOct 2025 - Phase 1/2Completed
Safety and Pilot Efficacy of AKB-9778 in Subjects With Diabetic Macular Edema
Subcutaneous AKB-9778
Diabetic Macular Edema (DME)
NCT01702441Enrollment24StartSep 2012Primary CompletionSep 2013CompletionDec 2014 - Phase 1/2Completed
Phase 1/2 Study of ABI-009 in Nonmuscle Invasive Bladder Cancer
ABI-009, Gemcitabine
Non-muscle Invasive Bladder Cancer (NMIBC)
NCT02009332Enrollment21StartApr 2014Primary CompletionDec 2019CompletionDec 2019 - Phase 1/2Completed
Nab-Sirolimus in Combination With FOLFOX & BEV as 1st Line Therapy in Patients With Advanced or Metastatic Colorectal Cancer
nab-sirolimus
Colorectal Cancer Metastatic
NCT03439462Enrollment60StartJul 2018Primary CompletionAug 2022CompletionAug 2022 - Phase 1Completed
Phase 1/1b Study With Nab-sirolimus for Patients With Severe Pulmonary Arterial Hypertension
nab-sirolimus
Pulmonary Hypertension
NCT02587325Enrollment15StartApr 2017Primary CompletionAug 2022CompletionSep 2022 - Phase 1Completed
Study to Assess the Absorption, Metabolism, Excretion and Pharmacokinetics of [14C]-AKB-9778
AKB-9778 subcutaneous injection
Healthy
NCT02858271Enrollment6StartJul 2016Primary CompletionJul 2016CompletionJul 2016 - Phase 1Completed
Single Ascending Dose Study to Assess the Safety, Tolerability, PK and PD Effects in Male Volunteers
AKB-4924
IBD
NCT02914262Enrollment40StartAug 2016Primary CompletionNov 2016CompletionJan 2017 - Phase 1Completed
Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AKB-9778 Ophthalmic Solution
AKB-9778 Ophthalmic Solution, Placebo Ophthalmic Solution
Ocular Hypertension, Primary Open Angle Glaucoma
NCT04284514Enrollment91StartMay 2019Primary CompletionDec 2019CompletionDec 2019 - Phase 1Completed
Dose-escalation Study to Assess Safety and Pharmacokinetics of Nab-Sirolimus in Patients With Locally Advanced or Metastatic Solid Tumors and Moderate Liver Impairment
nab-sirolimus
Tumor, Solid, Tumor +1
NCT05661461Enrollment15StartNov 2022Primary CompletionAug 2025CompletionSep 2026 - Phase 1Recruiting
Study Evaluating the Safety and Efficacy of HWK-007, a PTK7-directed Antibody Drug Conjugate in Participants With Advanced Solid Tumors
HWK-007
Endometrial Cancer, Ovarian Cancer +5
NCT07444814Enrollment226StartDec 2025Primary CompletionOct 2028est.CompletionDec 2028est. - Phase 1Recruiting
A Study of MUC16-Directed Antibody Drug Conjugate HWK-016 in Participants With Advanced Solid Tumors.
HWK-016, MUCIN-16-targeted ADC, Bevacizumab
PROC, Platinum Resistant Ovarian Cancer +1
NCT07470853Enrollment265StartMar 2026Primary CompletionFeb 2028est.CompletionFeb 2028est. - Expanded accessApproved for marketing
Expanded Access for ABI-009 in Patients With Advanced PEComa and Patients With a Malignancy With Relevant Genetic Mutations or mTOR Pathway Activation
ABI-009
PEComa, Malignant, TSC1 +2
NCT03817515Enrollment-Start-Primary Completion-Completion-
| Drug / Therapy | Link | ||
|---|---|---|---|
| Phase 2 | Completed | AKB-9778, ranibizumab | NCT02050828 |
| Phase 2 | Completed | AKB-9778 | NCT02387788 |
| Phase 2 | Completed | nab-Sirolimus | NCT02494570 |
| Phase 2 | Completed | nab-sirolimus, nab-sirolimus + temozolomide | NCT03463265 |
| Phase 2 | Withdrawn | ABI-009 | NCT03747328 |
| Phase 2 | Completed | nab-sirolimus | NCT05103358 |
| Phase 2 | Recruiting | nab-sirolimus | NCT05997017 |
| Phase 2 | Completed | nab-sirolimus | NCT05997056 |
| Phase 1/2 | Completed | Subcutaneous AKB-9778 | NCT01702441 |
| Phase 1/2 | Completed | ABI-009, Gemcitabine | NCT02009332 |
| Phase 1/2 | Completed | nab-sirolimus | NCT03439462 |
| Phase 1 | Completed | nab-sirolimus | NCT02587325 |
| Phase 1 | Completed | AKB-9778 subcutaneous injection | NCT02858271 |
| Phase 1 | Completed | AKB-4924 | NCT02914262 |
| Phase 1 | Completed | AKB-9778 Ophthalmic Solution, Placebo Ophthalmic Solution | NCT04284514 |
| Phase 1 | Completed | nab-sirolimus | NCT05661461 |
| Phase 1 | Recruiting | HWK-007 | NCT07444814 |
| Phase 1 | Recruiting | HWK-016, MUCIN-16-targeted ADC, Bevacizumab | NCT07470853 |
| Expanded access | Approved for marketing | ABI-009 | NCT03817515 |