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Heidelberg Pharma AG (HPHA) Drug Pipeline

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Drug pipeline
Drug NameConditionStageStatusStudy NameTrial Start DateArticle
Hdp-101Multiple Myeloma, Plasma Cell Disorderphase1AndPhase2RecruitingStudy to Assess Safety of HDP-101 in Patients With Relapsed Refractory Multiple MyelomaApr 23, 2021―
Iodine (124I) GirentuximabRenal Cell Carcinoma, Kidney CancerPhase IIIWithdrawnREDECT 2: REnal Masses: Pivotal Trial to DEteCT Clear Cell Renal Cell Carcinoma With PET/CTDec 19, 2012―
124-Iodine-Cg250 (124I-Cg250), CtRenal Cell Carcinoma, Kidney CancerPhase IIICompletedPre-surgical Detection of Clear Cell Renal Cell Carcinoma (ccRCC) Using Radiolabeled G250-AntibodyJan 21, 2008―
GirentuximabKidney CancerPhase IIICompletedMonoclonal Antibody Therapy (Rencarex®) in Treating Patients Who Have Undergone Surgery for Non-metastatic Kidney CancerJul 08, 2004―

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 Heidelberg Pharma AG (DE:HPHA) have in its pipeline
Heidelberg Pharma AG DE:HPHA is currently developing the following drugs: Hdp-101, Iodine (124I) Girentuximab, 124-Iodine-Cg250 (124I-Cg250), Ct, Girentuximab. These drug candidates are in various stages of clinical development as the company works toward FDA approval.