TipRanks
Go Ultimate55% OFF

Apollomics (APLM) Drug Pipeline

Drug pipeline
Drug NameConditionStageStatusStudy NameTrial Start DateArticle
UproleselanRelapsed/Refractory AmlPhase IIITerminatedStudy to Evaluate the Efficacy of Uproleselan in Combination With Chemotherapy in Chinese Patients With R/R AMLSep 14, 2021―
Apl-102 CapsulesAdvanced Solid TumorPhase ISuspendedAPL-102 Capsule in Patients With Advanced Solid TumorsAug 22, 2021―
UproleselanRelapsed/Refractory AmlPhase ICompletedStudy to Evaluate PK and Safety With Uproleselan Combined With Chemotherapy to Treat Chinese R/R AML PatientsMar 22, 2021―
Apl-101 Oral CapsulesSolid Tumors, Pancreatic Cancer, Renal Cancer, Lung Cancer, Gastric Cancer, Nsclc, Advanced Cancer, Glioblastoma Multiforme, Brain Tumor, Gastroesophageal Junction Adenocarcinoma, Colon Cancer, Thyroid Cancer, Egfr Gene Mutation, Met Amplification, Hgf, Met Alteration, Met Fusion, Exon 14 SkippingPhase IIRecruitingAPL-101 Study of Subjects With NSCLC With c-Met EXON 14 Skip Mutations and c-Met Dysregulation Advanced Solid TumorsJun 01, 2017―

FAQ

What are the FDA phases for drug approval?
The FDA approval process for new drugs is divided into several phases: a. Preclinical testing b. Phase 1 – Safety and dosage c. Phase 2 – Effectiveness and side effects d. Phase 3 – Confirmation of effectiveness, monitoring of adverse reactions, and comparison with existing treatments e. Phase 4 – Post-marketing studies to track long-term safety and effectiveness
What is a clinical trial?
A clinical trial is a carefully designed study in which researchers test a drug, treatment, or medical device in people to evaluate its safety, effectiveness, and potential side effects. These trials are essential for determining whether a new treatment should be approved for widespread use.
What drugs does Apollomics Inc. (APLM) have in its pipeline
Apollomics APLM is currently developing the following drugs: Uproleselan, Apl-102 Capsules, Apl-101 Oral Capsules. These drug candidates are in various stages of clinical development as the company works toward FDA approval.