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One article to understand what is ind application.

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Introduction to IND

IND, Investigational New Drug, generally refers to a new drug that has not been approved for marketing and is undergoing clinical trials at various stages. In actual applications, IND or CTA (clinical trial application) has become synonymous with pre-marketing human clinical trials. The IND application may be one or a sequential group of studies to obtain evidence of product safety and effectiveness. Generally speaking, INDs can be divided into commercial INDs and non-commercial INDs. Commercial INDs are for registration purposes and can distinguish between phase I and II clinical trials. Phase III clinical trials, or exploratory clinical trials and confirmatory clinical trials. . Commercial INDs are usually initiated by drug R&D applicants. Non-commercial INDs are usually not for registration purposes. Researchers mostly initiate them. It isn't easy to define whether they should be classified as exploratory clinical trials or confirmatory clinical trials.

FDA IND Filing

Where is the IND application in the development of new drugs?

Innovative drugs go through a systematic purgatory process full of thorns from structural design, discovery, and finally, approval to market. Briefly, the first is the discovery of the new chemical entity NCE, which mainly includes the identification of lead compounds and candidate drugs; after that, it enters the pre-clinical research stage, which provides for primary pharmacology, toxicology, pharmacokinetics, pre-prescription research, etc. After completing the preliminary pre-clinical evaluation and about to enter the clinical study, the development company applicant must apply for registration to the corresponding drug review department. This node is the content of this article~IND application; the pending drug review department passes the IND application, or When there is no feedback, the project enters the next phase, namely phase I, II, and III clinical research; after the pre-clinical research and clinical research are completed or partly completed if the common purpose is achieved, the new drug marketing application NDA can be submitted. To be approved for marketing after the listing, the development company still needs to conduct phase IV clinical research and post-marketing monitoring of the product so that it can fully understand the drug's mechanism, scope, therapeutic effect, and side effects.

What information will the IND review evaluate?

☆Background information for registration application

The background information to be considered in an IND application mainly includes four parts: the structural source of the compound, the pharmacological classification, the current status of research/marketing of similar drugs at home and abroad, and the prior position of the application project. Among them, the structure source mainly analyzes whether the compound is a new structure, an existing core structure modification, or a salt or ester of a marketed drug; the pharmacological classification is mainly combined with the research information provided by the Applicant to determine whether it is a new mechanism, a new target or a new target. There is a mechanism or target of a drug. The above two points can be used to make preliminary judgments on its druggability and risk. For example, for compounds with new structures, mechanisms, and targets, the hidden development risk is much higher than the salt or ester formation of the marketed drugs. The possibility of being a medicine is also relatively low.

☆Target indications and unmet clinical needs

On the one hand, it may increase the availability of medicines, and on the other hand, it may solve the problems of existing medication. Therefore, it is necessary to fully understand the target indications, including epidemiological evidence, disease severity and prognosis, current treatment methods and their shortcomings, and the development trend and experience of target indication drugs. In addition, it is necessary to understand the appropriate diagnosis and treatment guidelines, drug development trends, the potential of the varieties under application, etc.

☆Overall development ideas and plans

The main concern is whether the Applicant has formulated the overall plan of the human trial research path, at which stage the applied research is in the planning, or whether there is no overall or phased research plan, only the application project itself has put forward the research questions/plans at a specific stage.

☆Clinical trials to be carried out

Understand the basic information of the application project, such as which phase/phase of human clinical trials to be carried out, including the amount of the sample, the duration of the trial, the dosing plan, the research scale (location), etc., to provide for the follow-up technical evaluation Reference basis.

☆Key scientific evidence supporting the current application

Pay attention to the basis for supporting the current application, mainly considering validity. This supporting evidence primarily comes from clinical trials (in the process of clinical trials of a particular compound, new clinical applications may be discovered, and new Applications are often far from the expected initial indications), primary research (basic research starting from the laboratory is still the standard path for most drug development, if the supporting information comes from basic research, you need to pay attention to the evidence of this information Intensity) or other relevant information (in some cases, mainly when drugs with the exact mechanism of action have been successfully marketed and there is no reasonable model, bridging knowledge can be used to obtain supporting information for the application, such as mechanism research, drug metabolism Distribution of research information, etc.).

☆Evaluation of the integrity and scientificity of the research plan

Judging from the current international research trends, developing new drugs is a research evaluation model dominated by clinical trial programs. The staging of traditional clinical trials is becoming more and more obscure. Whether a drug can be marketed depends on whether the data obtained can support the evaluation of its safety and effectiveness rather than whether complete clinical trials have been carried out. The content and schedule of non-clinical and pharmaceutical research should be determined according to the content of the clinical trial to be carried out, and research and evaluation are accompanied by research and evaluation while making decisions. The scientific and overall assessment of the research program is mainly to evaluate the proposed clinical program. The content includes the primary research hypothesis, research population, efficacy indicators, research cycle, drug delivery method, basis, control bias means, data management, Applicant's risk control measures, etc.

☆Safety assessment

Based on the proposed clinical trial plan, evaluate the compound's research data, research data of similar compounds or drugs with the exact mechanism of action, and preparation-related safety information, and judge whether the existing data (self + literature) can support the safety of clinical trials, And put forward the risk control points that may need attention. The risk mainly comes from research on the compound, similar compounds, and similar mechanisms.

☆Preparation of quality risk

Whether the quality of the test substance used in early clinical trials is comparable to the quality of the test substance used in non-clinical trials, and whether the quality of the test substance used in subsequent clinical trials is similar to the quality of the test substance used in the previous clinical trials, pay attention to the test substance The nature and content of impurities.

☆Risk control during clinical trials

Based on the above evaluation of the proposed clinical trial plan and safety information, analyze whether there are sufficient risk control measures in the clinical trial plan. The specific content includes: whether the subjects in the clinical trial design are healthy volunteers or select the corresponding patient group based on the safety risk signals and the clinical trial itself; for the known potential risks, whether the monitoring procedures are complete, whether the exposure can be effectively exposed and can be identified Safety signals, whether there are unacceptable system risks; whether the clinical trial plan has formulated the necessary risk control methods based on risk analysis; whether there is a mechanism for evaluating and improving the risk control methods.

☆Pharmaceutical Research

In the development of innovative drugs, pharmacy-related changes are almost inevitable, especially in the early development stage, where changes occur more frequently. Generally, in the pre-clinical and early clinical research stages, pharmaceutical research is mainly to provide quality-guaranteed research samples for the above analysis; with the advancement of clinical research, pharmaceutical research is committed to definite, stable, reproducible, and industrialized production Processes and building a complete drug quality control system; combing with clinical research/treatment needs, scale-up production needs, and continuous deepening of drug understanding, the dosage form, specifications, prescription process, analysis methods, quality standards, etc. are adjusted and optimized.

☆Technical conclusion

Summarize the background above and evaluative information, and judge whether the evidence currently obtained supports the Applicant's research plan. If it is supported, it is necessary to clarify the scope of clinical exploration supported, the corresponding risk prompts, the supportive research that needs to be further carried out in the follow-up, and other related aspects such as the work of PI, CRO, and ethics committee. If the existing evidence does not support the proposed clinical trial protocol, it is necessary to clarify the deficiencies and follow-up issues that should be paid attention to.

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