Recent Updates
Recently added Catalysts

HY1272

Phase 1

NSCLC Stage IV | Small molecule | Oncology |Genelux Corporation|Last Updated: Jan 23, 2024

Success Probability

Subscribe to view

Market & Valuation

Subscribe to view

Trial Design

UNCONTROLLED
Total Trials1
Total Enrollment40

FDA Designations

No designations recorded

Clinical trial landscape

HY1272 · 1 trial · 1 indication

Phase 1 1
NCT06218940HY1272 in Patients With Locally Advanced or Metastatic Solid Tumors or Locally Advanced or Metastatic EGFRm+ NSCLCNSCLC Stage IV
NOT YET_RECRUITING40 Analytics
PHASE1NOT YET_RECRUITING
HY1272 in Patients With Locally Advanced or Metastatic Solid Tumors or Locally Advanced or Metastatic EGFRm+ NSCLC
NSCLC Stage IVUnlock trial analytics

Study Endpoints

Primary Endpoints

Evalute safety, tolerability of HY1272 in patients from day 1 to end of study.
baseline to study end (24 months as planned)

Incidence and severity of various adverse events, including physical examination, blood routine, blood biochemistry, urine flow sediment test, coagulation function, vital signs (pulse, respiration, blood pressure, body temperature), electrocardiogram, etc

Evalute PK of HY1272 in patients from week 1 to week 3.
Week 1 to week 3.

Evaluate changes of Pharmacokinetics (PK) evaluation mainly Cmax from Week 1 to Week 3.

Unlock Study Endpoints

Study Design & Arms

AllocationNA
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
HY1272EXPERIMENTALHY1272 IV weekly

Interventions

NameTypeDescription
HY1272DRUGEach patient will receive HY1272 weely or HY1272 weely+Oshitinib 80mg P.O. daily
Unlock Study Design Details

Eligibility Criteria

Age Range18 Years to 65 Years
SexALL
Healthy VolunteersNo

Inclusion Criteria: 1. Provision of signed and dated written informed consent prior to any study-specific procedures, sampling, and analyses. If a patient declines to participate in any voluntary exploratory research and/or genetic component of the study, there will be no penalty or loss of benefit...

Unlock Eligibility Criteria

Frequently asked questions about HY1272

What is HY1272 used for?

HY1272 is an investigational small molecule being developed for the treatment of NSCLC Stage IV, specifically in patients with locally advanced or metastatic EGFRm+ non-small cell lung cancer. It is also being studied in patients with locally advanced or metastatic solid tumors.

Who makes HY1272?

HY1272 is being developed by Genelux Corporation, a biopharmaceutical company traded on the stock exchange under the ticker symbol GNLX. The company is conducting clinical research to evaluate the safety and efficacy of this investigational drug.

What phase is HY1272 in?

HY1272 is currently in Phase 1 clinical development. It is an investigational drug, meaning it has not yet been approved by regulatory authorities and is still undergoing clinical trials to assess its safety and effectiveness in patients.

What clinical trials is HY1272 in?

HY1272 is being studied in a Phase 1 clinical trial with the identifier NCT06218940. This trial is titled 'HY1272 in Patients With Locally Advanced or Metastatic Solid Tumors or Locally Advanced or Metastatic EGFRm+ NSCLC' and is currently not yet recruiting participants.

How does HY1272 work?

The specific molecular target of HY1272 has not been disclosed in available information. As a small molecule, it is designed to interact with cellular components to exert its therapeutic effect, but the exact mechanism of action is not publicly detailed at this time.