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Juniper JN0-360 : Juniper Networks Certified Internet Specialist SP Exam

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Test Number : JN0-360
Test Name : Juniper Networks Certified Internet Specialist SP
Vendor Name : Juniper
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JN0-360 test Format | JN0-360 Course Contents | JN0-360 Course Outline | JN0-360 test Syllabus | JN0-360 test Objectives


Exam Name : Service Provider Routing and Switching Specialist
Exam Number : JN0-361 JNCIS-SP
Exam Duration : 90 minutes
Questions in test : 65
Passing Score : Variable (60-70% Approx.)
Recommended Training : Junos Intermediate Routing (JIR)
Junos Service Provider Switching (JSPX)
Junos MPLS Fundamentals (JMF)
Exam Registration : PEARSON VUE
Real Questions : Juniper JN0-361 Real Questions
VCE practice test : Juniper Networks Certified Specialist Service Provider Routing and Switching Practice Test

Protocol-Independent Routing
Identify the concepts, operation and functionality of various protocol-independent routing components
- Static, aggregate, and generated routes
- Martian addresses
- Routing instances, including RIB groups
- Load balancing
- Filter-based forwarding Demonstrate knowledge of how to configure and monitor various protocol-independent routing components
- Static, aggregate, and generated routes
- Load balancing
- Filter-based forwarding

Open Shortest Path First (OSPF)
Identify the concepts, operation and functionality of OSPF
- Link-state database
- OSPF packet types
- Router ID
- Adjacencies and neighbors
- Designated router (DR) and backup designated router (BDR)
- OSPF area and router types
- LSA packet types

Demonstrate knowledge of how to configure, monitor and troubleshoot OSPF
- Areas, interfaces and neighbors
- Additional basic options
- Routing policy application
- Troubleshooting tools

Intermediate System to Intermediate System (IS-IS)
Identify the concepts, operation and functionality of IS-IS
- Link-state database
- IS-IS PDUs
- TLVs
- Levels and areas
- Designated intermediate system (DIS)
- Metrics

Demonstrate knowledge of how to configure, monitor and troubleshoot OSPF
- Areas, interfaces and neighbors
- Additional basic options
- Routing policy application
- Troubleshooting tools

Border Gateway Protocol (BGP)
Identify the concepts, operation and functionality of BGP
- BGP basic operation
- BGP message types
- Attributes
- Route/path selection process
- IBGP and EBGP functionality and interaction

Demonstrate knowledge of how to configure and monitor BGP
- Groups and peers
- Additional basic options
- Routing policy application

Layer 2 Bridging and VLANs
Identify the concepts, operation, and functionality of Layer 2 bridging for the Junos OS
- Service Provider switching platforms
- Bridging elements and terminology
- Frame processing
- Virtual Switches
- Provider bridging (e.g., Q-in-Q tunneling)

Identify the concepts, benefits, and functionality of VLANs
- Port modes
- Tagging
- MVRP
- IRB

Demonstrate knowledge of how to configure, monitor and troubleshoot Layer 2 bridging and VLANs
- Interfaces and ports
- VLANs
- MVRP
- IRB
- Provider bridging

Spanning-Tree Protocols
Identify the concepts, benefits, operation, and functionality of Spanning Tree Protocol and its variants
- STP, RSTP, MSTP and VSTP concepts
- Port roles and states
- BPDUs
- Convergence and reconvergence
- Spanning-tree security

Demonstrate knowledge of how to configure, monitor and troubleshoot STP and its variants
- Spanning-tree protocols - STP, RSTP, MSTP, VSTP
- BPDU, loop and root protection

Multiprotocol Label Switching (MPLS) and MPLS VPNs
Identify the concepts, operation, and functionality of MPLS
- MPLS terminology
- MPLS packet header
- End-to-end packet flow and forwarding
- Labels and the label information base (LIB)
- MPLS and routing tables
- RSVP
- LDP

Identify the concepts, benefits, operation, and functionality of MPLS VPNs
- VPN routing tables
- Layer 3 VPN terminology and components
=> - BGP Layer 2 VPN terminology and components
- LDP Layer 2 circuit terminology and components
- Virtual private LAN service (VPLS) terminology and components
- MPLS VPN control plane traffic flow
- MPLS VPN data plane traffic flow

Demonstrate knowledge of how to configure and monitor MPLS
=> - MPLS forwarding
- RSVP-signaled and LDP-signaled LSPs

IPv6
Identify the concepts, operation and functionality of IPv6
- IPv4 vs. IPv6
- Address types, notation and format
- Address scopes
- Autoconfiguration
- Tunneling

Demonstrate knowledge of how to configure and monitor IPv6
- Interfaces
- Static routes
- Dynamic routing - OSPFv3, IS-IS, BGP
- IPv6 over IPv4 tunneling

Tunnels
Identify the concepts, requirements and functionality of IP tunneling
- Tunneling applications and considerations
- GRE
- IP-IP

Demonstrate knowledge of how to configure and monitor IP tunnels
- GRE configuration
- IP-IP configuration

High Availability
Identify the concepts, benefits, applications and requirements of high availability
- Link aggregation groups (LAG) and multichassis LAGs (MC-LAGs)
- Graceful restart (GR)
- Graceful Routing Engine switchover (GRES)
- Nonstop active routing (NSR)
- Nonstsop bridging (NSB)
- Bidirectional Forwarding Detection (BFD)
- Virtual Router Redundancy Protocol (VRRP)
- Unified In-Service Software Upgrade (ISSU)
- Ethernet Ring Protection (ERP)

Demonstrate knowledge of how to configure and monitor high availability component
- LAG, MC-LAG
- Additional basic options
- GR, GRES, NSR and NSB
- VRRP
=> - ISSU



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Juniper information source

Revance pronounces ultimate patient Enrolled in Modified JUNIPER part 2 upper Limb Spasticity Trial of DaxibotulinumtoxinA for Injection | JN0-360 test dumps and Dumps

The MarketWatch news department changed into not worried within the creation of this content.

Revance Therapeutics, Inc. (Nasdaq: RVNC), a biotechnology enterprise focused on imaginitive aesthetic and therapeutic choices, together with its next-era neuromodulator product, DaxibotulinumtoxinA for Injection, nowadays introduced a choice to finished enrollment in its JUNIPER section 2 trial of DaxibotulinumtoxinA for Injection for the medicine of higher limb spasticity in adults after stroke or tense brain harm. because of ongoing COVID-19 issues regarding area enrollment and scheduling in-adult examine visits, the company has chosen to conclusion screening and complete the analyze with 76 courses enrolled, along with just a few courses at the moment being evaluated for participation within the study. The 73 courses dosed earlier than enrollment was paused in March because of COVID-19 can be adopted for as much as 36 weeks; subjects enrolled after this should be adopted to Week 12. Revance now expects to announce topline data from the JUNIPER phase 2 trial in early 2021.

“In announcing the shut of enrollment for their JUNIPER phase 2 trial, we're taking a realistic strategy and making a proactive choice in mild of the continuing COVID-19 pandemic,” talked about Roman Rubio, M.D., Senior vice chairman of scientific construction at Revance. “happily, they have enrolled about two-thirds of the initial target topics, as a way to produce part 2 trial statistics that gives adequate suggestions to advance their scientific application in higher limb spasticity.”

brought Mark Foley, President and Chief government Officer, “while the enormous majority of their clinical development courses for DaxibotulinumtoxinA for Injection were unaffected by using the coronavirus pandemic, the one exception has been their JUNIPER trial, as in the past communicated. They introduced a pause in enrollment due to challenges in ongoing recruitment and subject monitoring as a result of social distancing. As COVID-linked concerns have persisted, they reassessed their assumptions and timeline, concluding that truncating the part 2 trial now might potentially permit us to circulate into the pivotal part three upper limb spasticity trials earlier than initially deliberate, while also keeping off affected person enrollment all through this difficult time.”

nowadays’s announcement capacity Revance’s therapeutic courses for DaxibotulinumtoxinA for Injection will generate three topline scientific consequences near time period: A section 3 pivotal trial in cervical dystonia; a phase 2 trial in plantar fasciitis; and a section 2 trial in upper limb spasticity. Concluded Foley, “We consider this enrollment determination is superior for Revance’s higher limb spasticity application, in addition to for the sufferers they hope to treat, and they seem to be forward to announcing the readouts in three therapeutic indications within the coming months.”

About JUNIPER section 2 study

The business’s JUNIPER examine is a part 2, randomized, double-blind, placebo-controlled, parallel group, dose-ranging, multi-core trial to evaluate the efficacy and security of DaxibotulinumtoxinA for Injection for the remedy of higher limb spasticity in adults following stroke or disturbing mind damage. The examine is being performed at 28 sites within the united states and has enrolled male and female sufferers between the age of 18 to seventy five years historic. patients had been randomized into one among 4 medication organizations: low dose, medium doses, high dose and a placebo. The analyze became designed to run for as much as 36 weeks, with two simple result measures: exchange from baseline in muscle community most severely affected by spasticity rating at Week 6; and change from Baseline medical professional international affect of exchange ranking at Week 6. 5 secondary outcome measures are also covered within the examine to check muscle tone improvement and length of effect.

additional information about the JUNIPER part 2 look at can also be found at www.clinicaltrials.gov using the identifier NCT03821402.

About Revance Therapeutics, Inc.

Revance Therapeutics, Inc. is a biotechnology enterprise focused on inventive aesthetic and therapeutic choices, together with its next-generation neuromodulator product, DaxibotulinumtoxinA for Injection. DaxibotulinumtoxinA for Injection combines a proprietary stabilizing peptide excipient with a particularly purified botulinum toxin that doesn't contain human or animal-primarily based accessories. Revance has efficiently completed a part three application for DaxibotulinumtoxinA for Injection in glabellar (frown) traces and is pursuing U.S. regulatory approval in 2020. Revance is additionally evaluating DaxibotulinumtoxinA for Injection in the full higher face, together with glabellar traces, forehead strains and crow’s ft, as well as in three therapeutic indications - cervical dystonia, adult upper limb spasticity and plantar fasciitis. beyond DaxibotulinumtoxinA for Injection, Revance has unique rights to commercialize TEOXANE SA’s Resilient Hyaluronic Acid® (RHA®) collection of dermal fillers in the U.S., the first and most effective latitude of FDA-authorized fillers for correction of dynamic facial wrinkles and folds. Revance additionally has an settlement with Mylan N.V. to Strengthen a biosimilar to BOTOX®, which would compete in the existing short-acting neuromodulator market. Revance is committed to creating a difference with the aid of reworking affected person experiences. For extra information or to be part of their team consult with us at www.revance.com.

“Revance Therapeutics” and the Revance emblem are registered emblems of Revance Therapeutics, Inc.Resilient Hyaluronic Acid® and RHA® are emblems of TEOXANE SA.BOTOX® is a registered trademark of Allergan, Inc.

forward-looking remark

This press release contains ahead-looking statements, together with statements involving Revance Therapeutics' 2020 monetary outlook, anticipated money runway and different monetary performance, the system and timing of, and means to comprehensive, latest and anticipated future scientific building of their investigational drug product candidates, the initiation, design, timing and consequences of their scientific studies, together with the SAKURA three analyze of DaxibotulinumtoxinA for Injection, section 3 application for treatment of cervical dystonia, section 2 and different medical classes for the management of plantar fasciitis and for the treatment of adult upper limb spasticity, and linked effects and reporting of such consequences; effects of their non-scientific classes; statements about their company approach, timeline and other desires and market for their anticipated items, plans and potentialities; including their pre-commercialization plans and timing of their advantage submission of a BLA submitting for DaxibotulinumtoxinA for Injection to deal with glabellar (frown) strains and capabilities regulatory method and product launch; statements about their ability to reap, and the timing relating to, regulatory approval with admire to their drug product candidates; statements related to additional milestone payments via their partnerships, and capabilities advantages of their drug product candidates and their excipient peptide and different applied sciences.

ahead-looking statements are field to hazards and uncertainties that may trigger genuine effects to vary materially from their expectations. These dangers and uncertainties encompass, but don't seem to be constrained to: the influence, can charge, and timing of their product building actions and medical trials; the uncertain medical development method, including the risk that clinical trials may also not have an effective design or generate high-quality consequences; their means to attain and hold regulatory approval of their drug product candidates; their capacity to achieve funding for their operations; their plans to research, improve, and commercialize their drug product candidates; their capacity to obtain market acceptance of their drug product candidates; unanticipated costs or delays in analysis, building, and commercialization efforts; the applicability of clinical examine effects to precise outcomes; the measurement and growth knowledge of the markets for their drug product candidates; their capacity to effectively commercialize their drug product candidates and the timing of commercialization activities; the cost and diploma of market acceptance of their drug product candidates; their ability to strengthen sales and advertising capabilities; the accuracy of their estimates concerning charges, future revenues, capital requirements and needs for financing; their skill to continue acquiring and maintaining intellectual property protection for their drug product candidates; and other dangers. distinctive guidance concerning elements that could cause precise results to vary materially from the consequences expressed or implied by statements during this press unencumber may well be present in Revance's periodic filings with the Securities and exchange commission (the "SEC"), together with factors described within the section entitled "chance factors" of their annual document on kind 10-k filed may 8, 2020. These ahead-searching statements communicate best as of the date hereof. Revance disclaims any responsibility to replace these forward-searching statements.

View source edition on businesswire.com: https://www.businesswire.com/news/domestic/20200630005831/en/

source: Revance Therapeutics, Inc.

MediaRevance Therapeutics, Inc.:Sara Fahy, 949-887-4476sfahy@revance.com or regularly occurring Media:Y&R:Jenifer Slaw, 347-971-0906jenifer.slaw@12 months.com orTrade Media:Nadine Tosk, 504-453-8344nadinepr@gmail.comInvestorsRevance Therapeutics, Inc.:Jeanie Herbert, 714-325-3584jherbert@revance.com or Gilmartin neighborhood, LLC.:Laurence Watts, 619-916-7620laurence@gilmartinir.com

COMTEX_367552574/2456/2020-06-30T16:05:15

Is there an issue with this press unlock? Contact the source issuer Comtex at editorial@comtex.com. that you could also contact MarketWatch consumer service by means of their consumer center.

Copyright company Wire 2020

The MarketWatch information department was no longer concerned in the introduction of this content material.


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