Tag Archives: Drug Approval

EMA Publish Guideline on Hep C Therapies

EMA Publish Guideline on Hep C Therapies.

Full Text Here

This guideline provides guidance on the clinical development of compounds for the treatment of Chronic Hepatitis C (CHC), including directly acting antivirals (DAAs) as well as host targeting antivirals (HTA). It should be read in conjunction with updated and recognised clinical treatment guidelines. Various combination regimens, including a DAA or HTA together with peginterferon (pegIFN) and ribavirin, regimens with more than one DAA/HTA in combination with pegIFN + ribavirin, as well as regimens excluding either or both of these agents, are considered.
While the primary investigation of new DAA/HTA in combination with pegIFN + ribavirin in patients with genotype (GT) 1 remains important, it is recognised that other paths of drug development, focussing on wider or alternative populations, or other drug combinations (such as more than one DAA/HTA with or without ribavirin, or 2 DAA/HTAs in combination with pegIFN+ribavirin) are warranted and ongoing.
The guidelines emphasize the importance of new DAA/HTA for usage in special populations including patients with decompensated liver disease, patients pre/post transplantation, HCV/HIV co-infected patients, patients intolerant to pegIFN and/or ribavirin and patients with prior DAA experience.
When studying novel agents in combination with pegIFN and ribavirin, the comparator in pivotal trials should be a licensed first line recommended regimen; notwithstanding this, European regulators recognise the need for licensed DAA/HTAs from several classes, with different side effects profiles and resistance patterns, which is seen as a benefit per se. When studying novel drug combinations without pegIFN, it is recommended that patients previously failing therapy with pegIFN+ribavirin that do not have an immediate treatment need be avoided prior to obtaining proof-of-concept of sustained virological response (SVR), as the consequences of acquired drug resistance in terms of retreatment success has still not been investigated. For drugs to be used in combinations eschewing pegIFN, it is recognised that patients that do not tolerate pegIFN have no presently licensed therapeutic options and a probability of viral clearance close to zero. Thus, for licensure, response rates would be weighed in relation to this fact. Regarding special populations, the need to start trials as early as can safely be done for groups with an important unmet medical need (e.g., patients with decompensated liver disease or HCV/HIV coinfection) is emphasised.
Since the previous guidelines were adapted, host IL-28B genotype has emerged as a very important predictor of the efficacy of pegIFN, and it is recommended that stratification by IL28B genotype be employed whenever the studied drug regimen includes this drug.
Regarding future developments, proof-of-concept of SVR with treatment combination excluding pegIFN, as well as data on retreatment of patients that have failed therapy that has selected for DAA-resistant variants, but whose dominant population has subsequently reverted to wild-type, are eagerly awaited. Such data are likely to greatly impact regulatory considerations within the field. It is recognised that this is a rapidly moving therapeutic area, and that a further revision of these guidelines may be mandated within the foreseeable future.

For Assistance with Developing Hep C Therapies Click Here

Damien Bové is THE Drug Development and Regulatory Consultant (pharmaceutical or biotechnology), I work with my clients to define a drug development target, define a drug development strategy, define a regulatory strategy or define a commercial strategy. Our clients are generally raising funds or looking to license out their technology and we help them achieve it. If you want to know more don’t hesitate to get in touch.

Avoid Expensive Mistakes, Keep On Top of New and Changing Regulations for Free!

Sign up for the most value add free newsource you can get for free. We spend a huge amount of time and effort monitoring the main drug / device regulators websites for changes in the regulatory environment, and capture between 20 and 40 new regulations, rules and initiatives each month, and summaries them in a fantastic FREE monthly Regulatory and Market Round Up. You can Un-Subscribe at any time and we don not share your details with anybody. You can’t afford to miss out on this service. Just fill in the form below.

Fill Out the Short Form Below…


  1. (required)


  2. (valid email required)

“Please note that the pages on this website are designed to provide you with general information only. We make no warranties, representations or undertakings about any of its content. This includes the completeness, accuracy and fitness for any particular purpose, or the content of any third party site referred to or accessed through it. You are personally responsible for ensuring that the information is correct and we will not be held liable or accountable for any mistakes that occur.”

EMA Publish Guideline on Clinical Evaluation of Treatments for Hepatitis C

EMA Publish Guideline on Clinical Evaluation of Treatments for Hepatitis C

Full Text Here

This guideline provides guidance on the clinical development of compounds for the treatment of Chronic Hepatitis C (CHC), including directly acting antivirals (DAAs) as well as host targeting antivirals (HTA). It should be read in conjunction with updated and recognised clinical treatment guidelines. Various combination regimens, including a DAA or HTA together with peginterferon (pegIFN) and ribavirin, regimens with more than one DAA/HTA in combination with pegIFN + ribavirin, as well as regimens excluding either or both of these agents, are considered.
While the primary investigation of new DAA/HTA in combination with pegIFN + ribavirin in patients with genotype (GT) 1 remains important, it is recognised that other paths of drug development, focussing on wider or alternative populations, or other drug combinations (such as more than one DAA/HTA with or without ribavirin, or 2 DAA/HTAs in combination with pegIFN+ribavirin) are warranted and ongoing.
The guidelines emphasize the importance of new DAA/HTA for usage in special populations including patients with decompensated liver disease, patients pre/post transplantation, HCV/HIV co-infected patients, patients intolerant to pegIFN and/or ribavirin and patients with prior DAA experience.
When studying novel agents in combination with pegIFN and ribavirin, the comparator in pivotal trials should be a licensed first line recommended regimen; notwithstanding this, European regulators recognise the need for licensed DAA/HTAs from several classes, with different side effects profiles and resistance patterns, which is seen as a benefit per se. When studying novel drug combinations without pegIFN, it is recommended that patients previously failing therapy with pegIFN+ribavirin that do not have an immediate treatment need be avoided prior to obtaining proof-of-concept of sustained virological response (SVR), as the consequences of acquired drug resistance in terms of retreatment success has still not been investigated. For drugs to be used in combinations eschewing pegIFN, it is recognised that patients that do not tolerate pegIFN have no presently licensed therapeutic options and a probability of viral clearance close to zero. Thus, for licensure, response rates would be weighed in relation to this fact. Regarding special populations, the need to start trials as early as can safely be done for groups with an important unmet medical need (e.g., patients with decompensated liver disease or HCV/HIV coinfection) is emphasised, Since the previous guidelines were adapted, host IL-28B genotype has emerged as a very important predictor of the efficacy of pegIFN, and it is recommended that stratification by IL28B genotype be employed whenever the studied drug regimen includes this drug.
Regarding future developments, proof-of-concept of SVR with treatment combination excluding pegIFN, as well as data on retreatment of patients that have failed therapy that has selected for DAA-resistant variants, but whose dominant population has subsequently reverted to wild-type, are eagerly awaited. Such data are likely to greatly impact regulatory considerations within the field. It is recognised that this is a rapidly moving therapeutic area, and that a further revision of these guidelines may be mandated within the foreseeable future.

For Assistance with Planning The Development of Hepatitis C Therapies Click Here

Damien Bové is THE Drug Development and Regulatory Consultant (pharmaceutical or biotechnology), I work with my clients to define a drug development target, define a drug development strategy, define a regulatory strategy or define a commercial strategy. Our clients are generally raising funds or looking to license out their technology and we help them achieve it. If you want to know more don’t hesitate to get in touch.

Avoid Expensive Mistakes, Keep On Top of New and Changing Regulations for Free!

Sign up for the most value add free newsource you can get for free. We spend a huge amount of time and effort monitoring the main drug / device regulators websites for changes in the regulatory environment, and capture between 20 and 40 new regulations, rules and initiatives each month, and summaries them in a fantastic FREE monthly Regulatory and Market Round Up. You can Un-Subscribe at any time and we don not share your details with anybody. You can’t afford to miss out on this service. Just fill in the form below.

Fill Out the Short Form Below…


  1. (required)


  2. (valid email required)

“Please note that the pages on this website are designed to provide you with general information only. We make no warranties, representations or undertakings about any of its content. This includes the completeness, accuracy and fitness for any particular purpose, or the content of any third party site referred to or accessed through it. You are personally responsible for ensuring that the information is correct and we will not be held liable or accountable for any mistakes that occur.”

EMA Publishes Guideline on Clinical Evaluation of Medicinal Products for the Treatment of Chronic Hepatitis C

EMA Publishes Guideline on Clinical Evaluation of Medicinal Products for the Treatment of Chronic Hepatitis C

Full Text Here

This guideline provides guidance on the clinical development of compounds for the treatment of Chronic Hepatitis C (CHC), including directly acting antivirals (DAAs) as well as host targeting antivirals (HTA). It should be read in conjunction with updated and recognised clinical treatment guidelines. Various combination regimens, including a DAA or HTA together with peginterferon (pegIFN) and ribavirin, regimens with more than one DAA/HTA in combination with pegIFN + ribavirin, as well as regimens excluding either or both of these agents, are considered.
While the primary investigation of new DAA/HTA in combination with pegIFN + ribavirin in patients with genotype (GT) remains important, it is recognised that other paths of drug development, focussing on wider or alternative populations, or other drug combinations (such as more than one DAA/HTA with or without ribavirin, or DAA/HTAs in combination with pegIFN+ribavirin) are warranted and ongoing.
The guidelines emphasize the importance of new DAA/HTA for usage in special populations including patients with decompensated liver disease, patients pre/post transplantation, HCV/HIV co-infected patients, patients intolerant to pegIFN and/or ribavirin and patients with prior DAA experience.
When studying novel agents in combination with pegIFN and ribavirin, the comparator in pivotal trials should be a licensed first line recommended regimen; notwithstanding this, European regulators recognise the need for licensed DAA/HTAs from several classes, with different side effects profiles and resistance patterns, which is seen as a benefit per se. When studying novel drug combinations without pegIFN, it is recommended that patients previously failing therapy with pegIFN+ribavirin that do not have an immediate treatment need be avoided prior to obtaining proof-of-concept of sustained virological response (SVR), as the consequences of acquired drug resistance in terms of retreatment success has still not been investigated. For drugs to be used in combinations eschewing pegIFN, it is recognised that patients that do not tolerate pegIFN have no presently licensed therapeutic options and a probability of viral clearance close to zero. Thus, for licensure, response rates would be weighed in relation to this fact. Regarding special populations, the need to start trials as early as can safely be done for groups with an important unmet medical need (e.g., patients with decompensated liver disease or HCV/HIV coinfection) is emphasised,
Since the previous guidelines were adapted, host IL-28B genotype has emerged as a very important predictor of the efficacy of pegIFN, and it is recommended that stratification by IL28B genotype be employed whenever the studied drug regimen includes this drug.
Regarding future developments, proof-of-concept of SVR with treatment combination excluding pegIFN, as well as data on retreatment of patients that have failed therapy that has selected for DAA-resistant variants, but whose dominant population has subsequently reverted to wild-type, are eagerly awaited. Such data are likely to greatly impact regulatory considerations within the field. It is recognised that this is a rapidly moving therapeutic area, and that a further revision of these guidelines may be mandated within the foreseeable future.

For Assistance with Clinical Development Planning and Regulatory Strategy Click Here

Damien Bové is THE Drug Development and Regulatory Consultant (pharmaceutical or biotechnology), I work with my clients to define a drug development target, define a drug development strategy, define a regulatory strategy or define a commercial strategy. Our clients are generally raising funds or looking to license out their technology and we help them achieve it. If you want to know more don’t hesitate to get in touch.

Avoid Expensive Mistakes, Keep On Top of New and Changing Regulations for Free!

Sign up for the most value add free newsource you can get for free. We spend a huge amount of time and effort monitoring the main drug / device regulators websites for changes in the regulatory environment, and capture between 20 and 40 new regulations, rules and initiatives each month, and summaries them in a fantastic FREE monthly Regulatory and Market Round Up. You can Un-Subscribe at any time and we don not share your details with anybody. You can’t afford to miss out on this service. Just fill in the form below.

Fill Out the Short Form Below…


  1. (required)


  2. (valid email required)

“Please note that the pages on this website are designed to provide you with general information only. We make no warranties, representations or undertakings about any of its content. This includes the completeness, accuracy and fitness for any particular purpose, or the content of any third party site referred to or accessed through it. You are personally responsible for ensuring that the information is correct and we will not be held liable or accountable for any mistakes that occur.”

Drug Regulators, EMEA (EMA), Publish a Concept Paper on the Need For Guidance on Clinical Investigations of Medicinal Products in the Treatment of Diabetes Mellitus

Drug Regulators, EMEA (EMA), Publish a Concept Paper on the Need For Guidance on Clinical Investigations of Medicinal Products in the Treatment of Diabetes Mellitus.

Full Text Here

The current CHMP Note for guidance on clinical investigation of medicinal products in the treatment of diabetes mellitus CPMP/EWP/1080/00 was adopted by the CHMP in November 2002.  New aspects have emerged since then including:
- Paediatric regulation has been implemented and a need for specific trials in children and adolescents with diabetes is considered.
- A number of new medicines for diabetes have been approved.
- Some medicines have only limited long-term safety data and may be associated with an increased cardiovascular risk.
- The possibility to develop medicines for the prevention of diabetes has been proposed.
- Combination treatment studies, especially with insulin, become more and more complex.
Therefore, the points mentioned above may deserve discussion and a need to update the guidance has been identified.

Damien Bové is THE Drug Development and Regulatory Consultant (pharmaceutical or biotechnology), I work with my clients to define a drug development target, define a drug development strategy, define a regulatory strategy or define a commercial strategy. Our clients are generally raising funds or looking to license out their technology and we help them achieve it. If you want to know more don’t hesitate to get in touch.

Avoid Expensive Mistakes, Keep On Top of New and Changing Regulations for Free!

Sign up for the most value add free newsource you can get for free. We spend a huge amount of time and effort monitoring the main drug / device regulators websites for changes in the regulatory environment, and capture between 20 and 40 new regulattions, rules and initiatives each month, and summarise them in a fantastic FREE monthly Regulatory and Market Round Up. You can Un-Subscribe at any time and we don not share your details with anybody. You can’t afford to miss out on this service. Just fill in the form below.

First name

Phone #1

E-mail address

ida consultants freestrategyconsultation 515x64 Drug Regulators, EMEA (EMA), Publish a Concept Paper on the Need For Guidance on Clinical Investigations of Medicinal Products in the Treatment of Diabetes Mellitus

Free Strategy Consultation - Biotech Pharma Regualtory

“Please note that the pages on this website are designed to provide you with general information only. We make no warranties, representations or undertakings about any of its content. This includes the completeness, accuracy and fitness for any particular purpose, or the content of any third party site referred to or accessed through it. You are personally responsible for ensuring that the information is correct and we will not be held liable or accountable for any mistakes that occur.”

ida 100programme 515x64 LowRes Drug Regulators, EMEA (EMA), Publish a Concept Paper on the Need For Guidance on Clinical Investigations of Medicinal Products in the Treatment of Diabetes Mellitus