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Chemotherapy-induced anemia (CIA) is a frequent complication of cancer treatment that occurs when chemotherapy damages bone marrow, leading to reduced red blood cell production and impaired oxygen delivery in the body. According to Dana Elkhalifa et al., 2025, epidemiological studies indicate that anemia affects roughly 25% to almost 90% of cancer patients, reflecting its significant clinical burden. Current treatment options include erythropoiesis-stimulating agents, iron therapies, and blood transfusions to manage symptoms. The growing focus on targeted supportive therapies, improved safety outcomes, and personalized care is strengthening drug development efforts. According to the chemotherapy-induced anemia pipeline analysis by Expert Market Research, rising cancer prevalence and therapeutic advancements are expected to drive notable growth in the coming years.
Major companies involved in the chemotherapy-induced anemia pipeline analysis include Shenyang Sunshine Pharmaceutical Co., Ltd., Kind Pharmaceuticals LLC, and others.
Leading drugs currently in the pipeline include SSS06, AND017, SAL-0951, and others.
The strong pipeline growth is driven by novel erythropoiesis-stimulating agents, hypoxia-inducible factor stabilizers, and combination therapies improving hemoglobin response, safety profiles, and patient adherence across oncology treatment settings.
The Chemotherapy Induced Anemia Pipeline Analysis Report by Expert Market Research provides comprehensive insights into chemotherapy induced anemia therapeutics currently undergoing clinical trials. It covers various aspects related to the details of each of these drugs under development for chemotherapy induced anemia. The chemotherapy induced anemia report assessment includes the analysis of over 100 pipeline drugs and 50+ companies. The chemotherapy induced anemia pipeline landscape will include an analysis based on efficacy and safety measure outcomes published for the trials, including their adverse effects on patients suffering from the condition, and alignment with chemotherapy induced anemia treatment guidelines to ensure optimal care practices.
The assessment part will include a detailed analysis of each drug, drug class, clinical studies, phase type, drug type, route of administration, and ongoing product development activities related to chemotherapy induced anemia.

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Chemotherapy induced anemia is a common complication of cancer treatment caused by chemotherapy damaging bone marrow and reducing red blood cell production. It occurs when cytotoxic drugs suppress erythropoiesis or increase red blood cell destruction, leading to fatigue, weakness, and reduced oxygen delivery throughout the body.
Chemotherapy induced anemia treatment commonly uses erythropoiesis-stimulating agents, iron supplementation, blood transfusions, and supportive therapies aimed at restoring hemoglobin levels and improving oxygen transport in cancer patients. According to Alfredo Tartarone et al., 2023, darbepoetin alfa has demonstrated continued clinical relevance, supported by regulatory approvals for cancer-related anemia. It received United States Food and Drug Administration approval for chemotherapy induced anemia in March 2006, while the European Medicines Agency authorized its use in adult cancer patients in June 2001.
Chemotherapy-Induced Anemia remains a critical unmet need in oncology drug development. According to Dana Elkhalifa et al., 2025, global cancer-related anemia prevalence varied from 12.8% to 100% across 65,179 patients from 40 countries. Higher incidence was reported in lung (84.2%), pediatric (80.9%), gynecological (62.99%), and gastrointestinal cancers (57.4%). Composite anemia prevalence was 64.99% in multiple cancer types and 25.68% in solid tumors. Chemotherapy and radiotherapy significantly increased anemia incidence, with some post-treatment cohorts reaching 100%. Regional disparities were noted, especially in Africa, South America, and the MENA regions. These epidemiological trends underscore active pipeline opportunities.
This section of the report covers the analysis of chemotherapy induced anemia drug candidates based on several segmentations, including:
By Phase
The pipeline assessment report covers 50+ drug analyses based on phase:
By Drug Class
The chemotherapy induced anemia pipeline analysis report covers 50+ drug analyses based on drug classes:
By Route of Administration
The pipeline assessment report covers 50+ drug analyses based on the route of administration:
The report covers phase I, phase II, phase III, phase IV, and early-phase drugs. The coverage includes an in-depth analysis of each drug across these phases. According to EMR analysis, phase II, with 60% covers a major share of the total chemotherapy induced anemia clinical trials, highlighting strong mid-stage development. Phase I and IV each account for 20%, demonstrating active early and late-stage progress. This balanced distribution across phases indicates robust innovation, potentially accelerating treatment availability and positively impacting the market growth and patient outcomes.
The drug molecule categories covered under the chemotherapy induced anemia pipeline analysis include small molecules, peptides, and oligonucleotides. The chemotherapy induced anemia report provides a comparative analysis of the drug classes for each drug in various phases of clinical trials for chemotherapy induced anemia. Hypoxia‑inducible factor prolyl hydroxylase (HIF‑PH) inhibitors are a key drug class in the chemotherapy‑induced anemia (CIA) pipeline. For instance, Roxadustat, an oral HIF‑PH inhibitor, is under clinical development to enhance erythropoiesis and improve hemoglobin levels in patients with CIA.
The EMR report for the chemotherapy induced anemia pipeline covers the profile of key companies involved in clinical trials and their drugs under development. It provides a detailed chemotherapy induced anemia therapeutic assessment, analyzing the competitive dynamics of the clinical trial landscape. Below is the list of a few players involved in chemotherapy induced anemia clinical trials:
This section covers the detailed analysis of each drug under multiple phases, including phase I, phase II, phase III, phase IV, and emerging drugs for chemotherapy induced anemia. It includes product description, trial ID, study type, drug class, mode of administration, and recruitment status of chemotherapy induced anemia drug candidates.
SSS06 is a long-acting, highly glycosylated recombinant erythropoietin-based protein being developed by Shenyang Sunshine Pharmaceutical Co., LTD. for the treatment of chemotherapy-induced anemia in patients with non-myeloid malignancies. The ongoing Phase II multicenter study is evaluating the safety, tolerability, immunogenicity, pharmacokinetics, and preliminary efficacy of SSS06 injection. The drug is being administered subcutaneously at varying dose levels every three weeks. SSS06 is working by stimulating red blood cell production through erythropoietin receptor activation, aiming to improve hemoglobin levels and reduce anemia-related complications.
AND017 is an investigational oral drug being developed by Kind Pharmaceuticals LLC for the treatment of chemotherapy-induced anemia. The Phase 2 multicenter, randomized, open-label study is currently not yet recruiting and is examining the safety and efficacy of AND017 over a six-week treatment period in cancer patients receiving chemotherapy. AND017 is being administered as oral capsules three times weekly across multiple dose groups. The drug is being designed to improve hemoglobin levels by stimulating red blood cell production and supporting oxygen delivery. The study is aiming to evaluate optimal dosing, tolerability, and therapeutic response in anemia management.
SAL-0951 (Enarodustat Tablets) is an oral hypoxia-inducible factor prolyl hydroxylase inhibitor being developed by Shenzhen Salubris Pharmaceuticals Co., Ltd. for the treatment of chemotherapy-induced anemia in patients with non-myeloid malignancies. The ongoing Phase II multicenter, open-label clinical study is evaluating the safety, efficacy, and optimal dosing of SAL-0951 administered once daily, with dose adjustments based on hemoglobin levels. This phase is aiming to examine the drug’s ability to stimulate endogenous erythropoietin production, improve hemoglobin concentration, and maintain an acceptable safety profile, thereby supporting dose optimization and progression toward future Phase III clinical development.
*Please note that this is only a partial list; the complete list of drugs will be available in the full report.*
The Chemotherapy Induced Anemia Pipeline Analysis Report provides a strategic overview of the latest and future landscape of treatments for chemotherapy induced anemia. It provides necessary information for making informed investment decisions along with research, development, and strategic planning efforts. The stakeholders will benefit from the essential insights into chemotherapy induced anemia collaborations, regulatory environments, and potential growth opportunities.
*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*
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