Anytime I have ever sent King an email, I have ALWAYS received a response in 24-48 hours. The folks that email and then start freaking out if they don't receive a response in an hour need to remember that King is receiving a metric sh-t ton of email traffic to be able to answer right away, oh in addition to having to run the actual business, oh and actually have some kind of life besides running the business. Do YOU work nights in addition to your full-time job? Do you work weekends in addition to your full-time job? Just give it a little bit of time and you will hear back. My advice would be not to innundate King with emails like, "Have you shipped my order yet?" or "Did you get my money?" HOWEVER, even if you DO go full retard, you will STILL always get a response. As long as you order correctly, you won't have a need for communication. Just let King do his thing, wait a week and BOOM! It's go time when you get the mail the next day. Oh yeah baby.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its identifier (NCT number): NCT02913261
Contacts Contact: Novartis Pharmaceuticals +41613241111 @ Contact: Novartis Pharmaceuticals +81337978748 @
Show 105 Study Locations
Sponsors and Collaborators Novartis Pharmaceuticals Investigators Study Director: Novartis Pharmaceuticals Novartis Pharmaceuticals More Information Go to Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information
Responsible Party: Novartis Pharmaceuticals Identifier: NCT02913261 History of Changes Other Study ID Numbers: CINC424C2301
First Posted: September 23, 2016 Key Record Dates Last Update Posted: March 21, 2018 Last Verified: March 2018 Individual Participant Data (IPD) Sharing Statement: Plan to Share IPD: Undecided Plan Description: Novartis is committed to sharing with qualified external researchers, access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations.
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