Max Neeman International

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Max Neeman International Clinical research Based out of 6 regional offices, Max Neeman has access to hospitals and health care facilities across India.

Max Neeman – A leading Contract Research Organization (CRO) based out of India provides full range of clinical research services to global pharmaceutical, biotech and device Companies. Operational since 2001, Max Neeman has been awarded 250 trials for global sponsors across wide range of therapeutic areas. Max Neeman has been awarded ISO 9001:2008 certification by United Kingdom Accreditation Service (UKAS) for Site Management, Monitoring and Data Management. Max Neeman has been awarded ISO 27001 & ISO 14155 certification for ISMS (Information Security Management System) and trials in Medical Devices respectively. We are presently active in 175 sites in 31 cities with access to 900 ICH-GCP trained Investigators. Record of maintaining a patient retention rate between 98.1 to 98.4% across different therapeutic areas like clinical trials in COPD etc. Successfully completed 5 US FDA GCP Audits for highest enrollment globally.

15/12/2012

MPEF finally over!!!

12/12/2012

Exam time for MNI..

15/11/2011

Genzyme investigational Phase III MS drug meets co-primary endpoints

Genzyme has reported positive Phase III results of Alemtuzumab (Lemtrada) to treat multiple sclerosis (MS).

The randomized trial was designed to assess whether the investigational alemtuzumab could achieve efficacy and safety improvements over the approved interferon beta-1a (Rebif).

The trial enrolled patients who have experienced at least two relapses within the two years prior therapy .

The trial met two co-primary endpoints including a reduction in relapse rate and six months sustained accumulation of disability (SAD).

Genzyme president and CEO David Meeker said based on these positive results, they are on track to submit Lemtrada for review to US and EU regulatory authorities in the first quarter of 2012.

15/11/2011

Theravance reports COPD drug Phase 2a positive results:

Theravance has reported positive Phase 2a study results of its investigational inhaled long-acting muscarinic antagonist (LAMA) - TD-4208.

The aim of the double-blind, randomized and four-period study was to assess the bronchodilatory effect, pharmacokinetics, safety and tolerability of single inhaled doses of TD-4208 in patients with chronic obstructive pulmonary disease (COPD).

The trial enrolling 32 patients recieved TD-4208 (350 mcg and 700 mcg), ipratropium bromide and placebo, each administered as single doses via a nebulizer.

The study met the primary endpoint with a mean change from baseline in peak forced expiratory volume in one second (FEV1) compared to placebo.

The study also met the secondary endpoints, including the drug's safety and tolerability.

Theravance Research and Early Clinical Development senior vice president Mathai Mammen said they are encouraged by these positive Phase 2a results which support further development of TD-4208 in COPD.

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